Canonical Allele Identifier: CA390746366

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414074A>G (hg19) ; chr14:g.87947730A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947730A>G , CM000676.2:g.87947730A>G	GRCh38
NC_000014.8:g.88414074A>G , CM000676.1:g.88414074A>G	GRCh37
NC_000014.7:g.87483827A>G	NCBI36
NG_011853.2:g.50834T>C
NG_011853.3:g.50834T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1487T>C MANE Select	ENSP00000261304.2:p.Val496Ala
ENST00000261304.6:c.1487T>C	ENSP00000261304.2:p.Val496Ala
ENST00000393568.8:c.1418T>C	ENSP00000377198.4:p.Val473Ala
ENST00000393569.6:c.1409T>C	ENSP00000377199.2:p.Val470Ala
ENST00000544807.6:c.1319T>C	ENSP00000437513.2:p.Val440Ala
ENST00000555000.5:c.854T>C	ENSP00000450472.1:p.Val285Ala
ENST00000555179.1:c.204T>C
ENST00000557316.5:c.*885T>C	ENSP00000452314.1:n.*885T>C
NM_000153.3:c.1487T>C	NP_000144.2:p.Val496Ala
NM_001201401.1:c.1418T>C	NP_001188330.1:p.Val473Ala
NM_001201402.1:c.1409T>C	NP_001188331.1:p.Val470Ala
XM_011536618.1:c.1319T>C	XP_011534920.1:p.Val440Ala
XM_011536618.2:c.1319T>C	XP_011534920.1:p.Val440Ala
NM_000153.4:c.1487T>C MANE Select	NP_000144.2:p.Val496Ala
NM_001201401.2:c.1418T>C	NP_001188330.1:p.Val473Ala
NM_001201402.2:c.1409T>C	NP_001188331.1:p.Val470Ala