Canonical Allele Identifier: CA390753423

Gene: GALC

Linked Data

• gnomAD v4: 14-87988504-A-G
• MyVariant Identifiers: chr14:g.88454848A>G (hg19) ; chr14:g.87988504A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988504A>G , CM000676.2:g.87988504A>G	GRCh38
NC_000014.8:g.88454848A>G , CM000676.1:g.88454848A>G	GRCh37
NC_000014.7:g.87524601A>G	NCBI36
NG_011853.2:g.10060T>C
NG_011853.3:g.10060T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.215T>C MANE Select	ENSP00000261304.2:p.Val72Ala
ENST00000261304.6:c.215T>C	ENSP00000261304.2:p.Val72Ala
ENST00000393568.8:c.196-297T>C	ENSP00000377198.4:n.196-297T>C
ENST00000393569.6:c.137T>C	ENSP00000377199.2:p.Val46Ala
ENST00000474294.6:n.205T>C
ENST00000544807.6:c.47T>C	ENSP00000437513.2:p.Val16Ala
ENST00000554372.5:c.215T>C	ENSP00000451884.1:p.Val72Ala
ENST00000554916.5:n.94T>C
ENST00000555956.1:n.20T>C
ENST00000556879.5:c.275T>C	ENSP00000452208.1:n.275T>C
ENST00000557316.5:c.215T>C	ENSP00000452314.1:p.Val72Ala
ENST00000622264.4:c.205T>C
NM_000153.3:c.215T>C	NP_000144.2:p.Val72Ala
NM_001201401.1:c.196-297T>C	NP_001188330.1:n.196-297T>C
NM_001201402.1:c.137T>C	NP_001188331.1:p.Val46Ala
XM_011536618.1:c.47T>C	XP_011534920.1:p.Val16Ala
XM_011536618.2:c.47T>C	XP_011534920.1:p.Val16Ala
NM_000153.4:c.215T>C MANE Select	NP_000144.2:p.Val72Ala
NM_001201401.2:c.196-297T>C	NP_001188330.1:n.196-297T>C
NM_001201402.2:c.137T>C	NP_001188331.1:p.Val46Ala