Canonical Allele Identifier: CA390751656

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88450805G>C (hg19) ; chr14:g.87984461G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87984461G>C , CM000676.2:g.87984461G>C	GRCh38
NC_000014.8:g.88450805G>C , CM000676.1:g.88450805G>C	GRCh37
NC_000014.7:g.87520558G>C	NCBI36
NG_011853.2:g.14103C>G
NG_011853.3:g.14103C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.515C>G MANE Select	ENSP00000261304.2:p.Ala172Gly
ENST00000261304.6:c.515C>G	ENSP00000261304.2:p.Ala172Gly
ENST00000393568.8:c.446C>G	ENSP00000377198.4:p.Ala149Gly
ENST00000393569.6:c.437C>G	ENSP00000377199.2:p.Ala146Gly
ENST00000474294.6:n.505C>G
ENST00000544807.6:c.347C>G	ENSP00000437513.2:p.Ala116Gly
ENST00000554372.5:c.*264C>G	ENSP00000451884.1:n.*264C>G
ENST00000554916.5:n.394C>G
ENST00000556261.5:n.216C>G
ENST00000556879.5:c.575C>G	ENSP00000452208.1:n.575C>G
ENST00000557316.5:c.515C>G	ENSP00000452314.1:p.Ala172Gly
ENST00000622264.4:c.505C>G
NM_000153.3:c.515C>G	NP_000144.2:p.Ala172Gly
NM_001201401.1:c.446C>G	NP_001188330.1:p.Ala149Gly
NM_001201402.1:c.437C>G	NP_001188331.1:p.Ala146Gly
XM_011536618.1:c.347C>G	XP_011534920.1:p.Ala116Gly
XM_011536618.2:c.347C>G	XP_011534920.1:p.Ala116Gly
NM_000153.4:c.515C>G MANE Select	NP_000144.2:p.Ala172Gly
NM_001201401.2:c.446C>G	NP_001188330.1:p.Ala149Gly
NM_001201402.2:c.437C>G	NP_001188331.1:p.Ala146Gly