Canonical Allele Identifier: CA390746369

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414075C>A (hg19) ; chr14:g.87947731C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947731C>A , CM000676.2:g.87947731C>A	GRCh38
NC_000014.8:g.88414075C>A , CM000676.1:g.88414075C>A	GRCh37
NC_000014.7:g.87483828C>A	NCBI36
NG_011853.2:g.50833G>T
NG_011853.3:g.50833G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1486G>T MANE Select	ENSP00000261304.2:p.Val496Phe
ENST00000261304.6:c.1486G>T	ENSP00000261304.2:p.Val496Phe
ENST00000393568.8:c.1417G>T	ENSP00000377198.4:p.Val473Phe
ENST00000393569.6:c.1408G>T	ENSP00000377199.2:p.Val470Phe
ENST00000544807.6:c.1318G>T	ENSP00000437513.2:p.Val440Phe
ENST00000555000.5:c.853G>T	ENSP00000450472.1:p.Val285Phe
ENST00000555179.1:c.203G>T
ENST00000557316.5:c.*884G>T	ENSP00000452314.1:n.*884G>T
NM_000153.3:c.1486G>T	NP_000144.2:p.Val496Phe
NM_001201401.1:c.1417G>T	NP_001188330.1:p.Val473Phe
NM_001201402.1:c.1408G>T	NP_001188331.1:p.Val470Phe
XM_011536618.1:c.1318G>T	XP_011534920.1:p.Val440Phe
XM_011536618.2:c.1318G>T	XP_011534920.1:p.Val440Phe
NM_000153.4:c.1486G>T MANE Select	NP_000144.2:p.Val496Phe
NM_001201401.2:c.1417G>T	NP_001188330.1:p.Val473Phe
NM_001201402.2:c.1408G>T	NP_001188331.1:p.Val470Phe