Canonical Allele Identifier: CA390749247

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88442703C>G (hg19) ; chr14:g.87976359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976359C>G , CM000676.2:g.87976359C>G	GRCh38
NC_000014.8:g.88442703C>G , CM000676.1:g.88442703C>G	GRCh37
NC_000014.7:g.87512456C>G	NCBI36
NG_011853.2:g.22205G>C
NG_011853.3:g.22205G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.751G>C MANE Select	ENSP00000261304.2:p.Gly251Arg
ENST00000261304.6:c.751G>C	ENSP00000261304.2:p.Gly251Arg
ENST00000393568.8:c.682G>C	ENSP00000377198.4:p.Gly228Arg
ENST00000393569.6:c.673G>C	ENSP00000377199.2:p.Gly225Arg
ENST00000474294.6:n.741G>C
ENST00000477716.3:n.506G>C
ENST00000544807.6:c.583G>C	ENSP00000437513.2:p.Gly195Arg
ENST00000554916.5:n.630G>C
ENST00000555000.5:c.118G>C	ENSP00000450472.1:p.Gly40Arg
ENST00000557316.5:c.*149G>C	ENSP00000452314.1:n.*149G>C
ENST00000622264.4:c.741G>C
NM_000153.3:c.751G>C	NP_000144.2:p.Gly251Arg
NM_001201401.1:c.682G>C	NP_001188330.1:p.Gly228Arg
NM_001201402.1:c.673G>C	NP_001188331.1:p.Gly225Arg
XM_011536618.1:c.583G>C	XP_011534920.1:p.Gly195Arg
XM_011536618.2:c.583G>C	XP_011534920.1:p.Gly195Arg
NM_000153.4:c.751G>C MANE Select	NP_000144.2:p.Gly251Arg
NM_001201401.2:c.682G>C	NP_001188330.1:p.Gly228Arg
NM_001201402.2:c.673G>C	NP_001188331.1:p.Gly225Arg