Canonical Allele Identifier: CA2843045931

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934693G>T , CM000676.2:g.87934693G>T	GRCh38
NC_000014.8:g.88401037G>T , CM000676.1:g.88401037G>T	GRCh37
NC_000014.7:g.87470790G>T	NCBI36
NG_011853.2:g.63871C>A
NG_011853.3:g.63871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.*39C>A MANE Select	ENSP00000261304.2:n.*39C>A
ENST00000261304.6:c.*39C>A	ENSP00000261304.2:n.*39C>A
ENST00000393568.8:c.*39C>A	ENSP00000377198.4:n.*39C>A
ENST00000393569.6:c.*39C>A	ENSP00000377199.2:n.*39C>A
ENST00000544807.6:c.1744-694C>A	ENSP00000437513.2:n.1744-694C>A
ENST00000555000.5:c.1279-694C>A	ENSP00000450472.1:n.1279-694C>A
NM_000153.3:c.*39C>A	NP_000144.2:n.*39C>A
NM_001201401.1:c.*39C>A	NP_001188330.1:n.*39C>A
NM_001201402.1:c.*39C>A	NP_001188331.1:n.*39C>A
XM_011536618.1:c.*39C>A	XP_011534920.1:n.*39C>A
XM_011536618.2:c.*39C>A	XP_011534920.1:n.*39C>A
NM_000153.4:c.*39C>A MANE Select	NP_000144.2:n.*39C>A
NM_001201401.2:c.*39C>A	NP_001188330.1:n.*39C>A
NM_001201402.2:c.*39C>A	NP_001188331.1:n.*39C>A