Canonical Allele Identifier: CA390749822

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442829A>C (hg19) ; chr14:g.87976485A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976485A>C , CM000676.2:g.87976485A>C	GRCh38
NC_000014.8:g.88442829A>C , CM000676.1:g.88442829A>C	GRCh37
NC_000014.7:g.87512582A>C	NCBI36
NG_011853.2:g.22079T>G
NG_011853.3:g.22079T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.625T>G MANE Select	ENSP00000261304.2:p.Leu209Val
ENST00000261304.6:c.625T>G	ENSP00000261304.2:p.Leu209Val
ENST00000393568.8:c.556T>G	ENSP00000377198.4:p.Leu186Val
ENST00000393569.6:c.547T>G	ENSP00000377199.2:p.Leu183Val
ENST00000474294.6:n.615T>G
ENST00000477716.3:n.380T>G
ENST00000544807.6:c.457T>G	ENSP00000437513.2:p.Leu153Val
ENST00000554916.5:n.504T>G
ENST00000555000.5:c.-9T>G	ENSP00000450472.1:n.-9T>G
ENST00000557316.5:c.*23T>G	ENSP00000452314.1:n.*23T>G
ENST00000622264.4:c.615T>G
NM_000153.3:c.625T>G	NP_000144.2:p.Leu209Val
NM_001201401.1:c.556T>G	NP_001188330.1:p.Leu186Val
NM_001201402.1:c.547T>G	NP_001188331.1:p.Leu183Val
XM_011536618.1:c.457T>G	XP_011534920.1:p.Leu153Val
XM_011536618.2:c.457T>G	XP_011534920.1:p.Leu153Val
NM_000153.4:c.625T>G MANE Select	NP_000144.2:p.Leu209Val
NM_001201401.2:c.556T>G	NP_001188330.1:p.Leu186Val
NM_001201402.2:c.547T>G	NP_001188331.1:p.Leu183Val