Canonical Allele Identifier: CA130548
Gene: ALG13 HGNC NCBI

Linked Data

dbSNP Id: rs397514587
MyVariant Identifiers: chrX:g.110928287A>G (hg19) chrX:g.111685059A>G (hg38)
PubMed: PMID:22492991 PMID:25732998
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.111685059A>G , CM000685.2:g.111685059A>G GRCh38
NC_000023.10:g.110928287A>G , CM000685.1:g.110928287A>G GRCh37
NC_000023.9:g.110814943A>G NCBI36
NG_016238.1:g.8942A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000623622.2:c.339A>G ENSP00000485624.2:p.Ala113=
ENST00000699748.1:c.*308A>G ENSP00000514558.1:n.*308A>G
ENST00000394780.8:c.339A>G MANE Select ENSP00000378260.3:p.Ala113=
ENST00000636363.1:c.339A>G ENSP00000490681.1:p.Ala113=
ENST00000251943.8:c.27A>G ENSP00000251943.4:p.Ala9=
ENST00000371979.7:c.339A>G ENSP00000361047.3:p.Ala113=
ENST00000394780.7:c.339A>G ENSP00000378260.3:p.Ala113=
ENST00000436609.5:c.27A>G ENSP00000392990.2:p.Ala9=
ENST00000468657.5:c.*308A>G ENSP00000480638.2:n.*308A>G
ENST00000470971.5:c.*103A>G ENSP00000479424.2:n.*103A>G
ENST00000471924.5:c.416A>G ENSP00000484523.2:n.416A>G
ENST00000473389.5:c.339A>G ENSP00000480711.1:p.Ala113=
ENST00000482374.5:c.*204A>G ENSP00000479632.1:n.*204A>G
ENST00000482742.5:c.27A>G ENSP00000477513.1:p.Ala9=
ENST00000486353.5:c.339A>G ENSP00000426892.2:p.Ala113=
ENST00000487141.5:c.375A>G ENSP00000478130.1:p.Ala125=
ENST00000489033.5:c.*249A>G ENSP00000482257.2:n.*249A>G
ENST00000492038.5:c.*103A>G ENSP00000479483.1:n.*103A>G
ENST00000495283.5:c.*204A>G ENSP00000427093.3:n.*204A>G
ENST00000610588.4:c.105A>G ENSP00000479731.1:p.Ala35=
ENST00000621367.4:c.27A>G ENSP00000481509.1:p.Ala9=
ENST00000622986.3:c.339A>G ENSP00000485067.1:p.Ala113=
ENST00000622997.3:c.*308A>G ENSP00000485420.1:n.*308A>G
ENST00000623144.3:c.*308A>G ENSP00000485279.1:n.*308A>G
ENST00000623148.3:c.357A>G ENSP00000485658.1:n.357A>G
ENST00000623189.1:c.27A>G ENSP00000485392.1:p.Ala9=
ENST00000623255.1:c.330A>G ENSP00000485333.1:p.Ala110=
ENST00000624161.3:c.*103A>G ENSP00000485181.1:n.*103A>G
ENST00000624881.3:c.280A>G ENSP00000485093.1:p.Lys94Glu
NM_001039210.3:c.280A>G NP_001034299.3:p.Lys94Glu
NM_001099922.2:c.339A>G NP_001093392.1:p.Ala113=
NM_001168385.1:c.339A>G NP_001161857.1:p.Ala113=
NM_001257230.1:c.27A>G NP_001244159.1:p.Ala9=
NM_001257231.1:c.105A>G NP_001244160.1:p.Ala35=
NM_001257234.1:c.27A>G NP_001244163.1:p.Ala9=
NM_001257235.1:c.27A>G NP_001244164.1:p.Ala9=
NM_001257237.1:c.27A>G NP_001244166.1:p.Ala9=
NM_001257239.1:c.27A>G NP_001244168.1:p.Ala9=
NM_001257240.1:c.27A>G NP_001244169.1:p.Ala9=
NM_001257241.1:c.105A>G NP_001244170.1:p.Ala35=
NM_018466.4:c.339A>G NP_060936.1:p.Ala113=
NR_033125.1:n.336A>G
XM_005262191.3:c.27A>G XP_005262248.1:p.Ala9=
XM_006724693.2:c.339A>G XP_006724756.1:p.Ala113=
XM_006724695.2:c.339A>G XP_006724758.1:p.Ala113=
XM_006724697.2:c.27A>G XP_006724760.2:p.Ala9=
XM_006724698.2:c.27A>G XP_006724761.2:p.Ala9=
XM_011531028.1:c.339A>G XP_011529330.1:p.Ala113=
XM_011531029.1:c.339A>G XP_011529331.1:p.Ala113=
XM_011531030.1:c.339A>G XP_011529332.1:p.Ala113=
XM_011531031.1:c.27A>G XP_011529333.1:p.Ala9=
XM_011531032.1:c.27A>G XP_011529334.1:p.Ala9=
XM_011531033.1:c.27A>G XP_011529335.1:p.Ala9=
XR_938409.1:n.812A>G
NM_001039210.4:c.280A>G NP_001034299.3:p.Lys94Glu
NM_001168385.2:c.339A>G NP_001161857.1:p.Ala113=
NM_001257235.2:c.27A>G NP_001244164.1:p.Ala9=
NM_001257239.2:c.27A>G NP_001244168.1:p.Ala9=
NM_001257240.2:c.27A>G NP_001244169.1:p.Ala9=
NM_001257241.2:c.105A>G NP_001244170.1:p.Ala35=
NM_001324290.1:c.345A>G NP_001311219.1:p.Ala115=
NM_001324291.1:c.27A>G NP_001311220.1:p.Ala9=
NM_001324292.1:c.339A>G NP_001311221.1:p.Ala113=
NM_001324293.1:c.27A>G NP_001311222.1:p.Ala9=
NM_001324294.1:c.27A>G NP_001311223.1:p.Ala9=
NM_018466.5:c.339A>G NP_060936.1:p.Ala113=
NR_033125.2:n.336A>G
NR_136735.1:n.409A>G
NR_148693.1:n.440A>G
XM_006724693.3:c.339A>G XP_006724756.1:p.Ala113=
XM_006724697.3:c.27A>G XP_006724760.2:p.Ala9=
XM_006724698.3:c.27A>G XP_006724761.2:p.Ala9=
XM_011531028.2:c.339A>G XP_011529330.1:p.Ala113=
XM_011531030.2:c.339A>G XP_011529332.1:p.Ala113=
XM_011531033.3:c.27A>G XP_011529335.1:p.Ala9=
XM_017029846.1:c.339A>G XP_016885335.1:p.Ala113=
XM_017029847.1:c.339A>G XP_016885336.1:p.Ala113=
XM_017029848.1:c.339A>G XP_016885337.1:p.Ala113=
XM_017029849.1:c.339A>G XP_016885338.1:p.Ala113=
XM_017029850.2:c.339A>G XP_016885339.1:p.Ala113=
XM_017029851.1:c.-372A>G XP_016885340.1:n.-372A>G
XM_024452449.1:c.339A>G XP_024308217.1:p.Ala113=
XR_001755726.1:n.379A>G
XR_001755727.1:n.379A>G
XR_001755728.1:n.379A>G
NM_001039210.5:c.280A>G NP_001034299.3:p.Lys94Glu
NM_001099922.3:c.339A>G MANE Select NP_001093392.1:p.Ala113=
NM_001168385.3:c.339A>G NP_001161857.1:p.Ala113=
NM_001257230.2:c.27A>G NP_001244159.1:p.Ala9=
NM_001257235.3:c.27A>G NP_001244164.1:p.Ala9=
NM_001257239.3:c.27A>G NP_001244168.1:p.Ala9=
NM_001257240.3:c.27A>G NP_001244169.1:p.Ala9=
NM_001257241.3:c.105A>G NP_001244170.1:p.Ala35=
NM_001324290.2:c.345A>G NP_001311219.1:p.Ala115=
NM_001324291.2:c.27A>G NP_001311220.1:p.Ala9=
NM_001324292.2:c.339A>G NP_001311221.1:p.Ala113=
NM_001324294.2:c.27A>G NP_001311223.1:p.Ala9=
NM_018466.6:c.339A>G NP_060936.1:p.Ala113=
NR_033125.3:n.284A>G
NR_136735.2:n.409A>G
NR_148693.2:n.388A>G
NM_001257231.2:c.105A>G NP_001244160.1:p.Ala35=
NM_001257234.2:c.27A>G NP_001244163.1:p.Ala9=
NM_001257237.2:c.27A>G NP_001244166.1:p.Ala9=
Search 100 bp 5'
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