Canonical Allele Identifier: CA390746444

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414107G>T (hg19) ; chr14:g.87947763G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947763G>T , CM000676.2:g.87947763G>T	GRCh38
NC_000014.8:g.88414107G>T , CM000676.1:g.88414107G>T	GRCh37
NC_000014.7:g.87483860G>T	NCBI36
NG_011853.2:g.50801C>A
NG_011853.3:g.50801C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1454C>A MANE Select	ENSP00000261304.2:p.Pro485His
ENST00000261304.6:c.1454C>A	ENSP00000261304.2:p.Pro485His
ENST00000393568.8:c.1385C>A	ENSP00000377198.4:p.Pro462His
ENST00000393569.6:c.1376C>A	ENSP00000377199.2:p.Pro459His
ENST00000544807.6:c.1286C>A	ENSP00000437513.2:p.Pro429His
ENST00000555000.5:c.821C>A	ENSP00000450472.1:p.Pro274His
ENST00000555179.1:c.171C>A
ENST00000557316.5:c.*852C>A	ENSP00000452314.1:n.*852C>A
NM_000153.3:c.1454C>A	NP_000144.2:p.Pro485His
NM_001201401.1:c.1385C>A	NP_001188330.1:p.Pro462His
NM_001201402.1:c.1376C>A	NP_001188331.1:p.Pro459His
XM_011536618.1:c.1286C>A	XP_011534920.1:p.Pro429His
XM_011536618.2:c.1286C>A	XP_011534920.1:p.Pro429His
NM_000153.4:c.1454C>A MANE Select	NP_000144.2:p.Pro485His
NM_001201401.2:c.1385C>A	NP_001188330.1:p.Pro462His
NM_001201402.2:c.1376C>A	NP_001188331.1:p.Pro459His