Canonical Allele Identifier: CA390746432

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414102G>C (hg19) ; chr14:g.87947758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947758G>C , CM000676.2:g.87947758G>C	GRCh38
NC_000014.8:g.88414102G>C , CM000676.1:g.88414102G>C	GRCh37
NC_000014.7:g.87483855G>C	NCBI36
NG_011853.2:g.50806C>G
NG_011853.3:g.50806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1459C>G MANE Select	ENSP00000261304.2:p.Pro487Ala
ENST00000261304.6:c.1459C>G	ENSP00000261304.2:p.Pro487Ala
ENST00000393568.8:c.1390C>G	ENSP00000377198.4:p.Pro464Ala
ENST00000393569.6:c.1381C>G	ENSP00000377199.2:p.Pro461Ala
ENST00000544807.6:c.1291C>G	ENSP00000437513.2:p.Pro431Ala
ENST00000555000.5:c.826C>G	ENSP00000450472.1:p.Pro276Ala
ENST00000555179.1:c.176C>G
ENST00000557316.5:c.*857C>G	ENSP00000452314.1:n.*857C>G
NM_000153.3:c.1459C>G	NP_000144.2:p.Pro487Ala
NM_001201401.1:c.1390C>G	NP_001188330.1:p.Pro464Ala
NM_001201402.1:c.1381C>G	NP_001188331.1:p.Pro461Ala
XM_011536618.1:c.1291C>G	XP_011534920.1:p.Pro431Ala
XM_011536618.2:c.1291C>G	XP_011534920.1:p.Pro431Ala
NM_000153.4:c.1459C>G MANE Select	NP_000144.2:p.Pro487Ala
NM_001201401.2:c.1390C>G	NP_001188330.1:p.Pro464Ala
NM_001201402.2:c.1381C>G	NP_001188331.1:p.Pro461Ala