Canonical Allele Identifier: CA246547

Linked Data

ClinVar Variation Id: 198058
dbSNP Id: rs104894635

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80213815C>A , CM000679.2:g.80213815C>A GRCh38
NC_000017.10:g.78187614C>A , CM000679.1:g.78187614C>A GRCh37
NC_000017.9:g.75802209C>A NCBI36
NG_008229.1:g.11586G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703570.1:n.2845-2051C>A (CARD14)
ENST00000326317.11:c.734G>T (SGSH) MANE Select ENSP00000314606.6:p.Arg245Leu
ENST00000326317.10:c.734G>T (SGSH) ENSP00000314606.6:p.Arg245Leu
ENST00000570923.1:c.769G>T (SGSH) ENSP00000458200.1:p.Ala257Ser
ENST00000572257.5:c.336G>T (SGSH)
ENST00000573150.5:c.628G>T (SGSH) ENSP00000459280.1:p.Ala210Ser
ENST00000575282.5:n.1029G>T (SGSH)
ENST00000576941.5:c.*150G>T (SGSH) ENSP00000461160.1:n.*150G>T
NM_000199.3:c.734G>T (SGSH) NP_000190.1:p.Arg245Leu
XM_005257582.2:c.734G>T (SGSH) XP_005257639.1:p.Arg245Leu
XM_005257583.3:c.734G>T (SGSH) XP_005257640.1:p.Arg245Leu
XM_011525126.1:c.734G>T (SGSH) XP_011523428.1:p.Arg245Leu
XM_011525127.1:c.734G>T (SGSH) XP_011523429.1:p.Arg245Leu
XR_934532.1:n.754G>T (SGSH)
NM_000199.4:c.734G>T (SGSH) NP_000190.1:p.Arg245Leu
NM_001352921.1:c.734G>T (SGSH) NP_001339850.1:p.Arg245Leu
NM_001352922.1:c.734G>T (SGSH) NP_001339851.1:p.Arg245Leu
NR_148201.1:n.715G>T (SGSH)
XM_005257583.4:c.734G>T (SGSH) XP_005257640.1:p.Arg245Leu
XM_017024952.1:c.734G>T (SGSH) XP_016880441.1:p.Arg245Leu
XR_001752585.1:n.754G>T (SGSH)
XR_001752586.1:n.754G>T (SGSH)
XR_001752587.1:n.754G>T (SGSH)
XR_001752588.1:n.754G>T (SGSH)
XR_001752589.1:n.754G>T (SGSH)
XR_001752590.1:n.754G>T (SGSH)
XR_001752591.1:n.754G>T (SGSH)
XR_001752592.1:n.754G>T (SGSH)
XR_002958057.1:n.754G>T (SGSH)
XR_934532.2:n.754G>T (SGSH)
NM_000199.5:c.734G>T (SGSH) MANE Select NP_000190.1:p.Arg245Leu
NM_001352921.2:c.734G>T (SGSH) NP_001339850.1:p.Arg245Leu
NM_001352922.2:c.734G>T (SGSH) NP_001339851.1:p.Arg245Leu
NR_148201.2:n.648G>T (SGSH)
NM_001352921.3:c.734G>T (SGSH) NP_001339850.1:p.Arg245Leu