Canonical Allele Identifier: CA384387383
Gene: ALG10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.34179770A>C (hg19) chr12:g.34026835A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.34026835A>C , CM000674.2:g.34026835A>C GRCh38
NC_000012.11:g.34179770A>C , CM000674.1:g.34179770A>C GRCh37
NC_000012.10:g.34071037A>C NCBI36
NG_016389.1:g.9555A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266483.7:c.1342A>C MANE Select ENSP00000266483.2:p.Asn448His
ENST00000266483.6:c.1342A>C ENSP00000266483.2:p.Asn448His
ENST00000538927.1:c.369+2676A>C ENSP00000444084.1:n.369+2676A>C
ENST00000541875.1:c.*1082A>C ENSP00000443142.1:n.*1082A>C
NM_032834.3:c.1342A>C NP_116223.3:p.Asn448His
XM_024449230.1:c.1162A>C XP_024304998.1:p.Asn388His
XM_024449231.1:c.1162A>C XP_024304999.1:p.Asn388His
NM_032834.4:c.1342A>C MANE Select NP_116223.3:p.Asn448His
Search 100 bp 5'
Search 100 bp 3'