Canonical Allele Identifier: CA390745073

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88401078A>T (hg19) ; chr14:g.87934734A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934734A>T , CM000676.2:g.87934734A>T	GRCh38
NC_000014.8:g.88401078A>T , CM000676.1:g.88401078A>T	GRCh37
NC_000014.7:g.87470831A>T	NCBI36
NG_011853.2:g.63830T>A
NG_011853.3:g.63830T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.2056T>A MANE Select	ENSP00000261304.2:p.Ter686Lys
ENST00000261304.6:c.2056T>A	ENSP00000261304.2:p.Ter686Lys
ENST00000393568.8:c.1987T>A	ENSP00000377198.4:p.Ter663Lys
ENST00000393569.6:c.1978T>A	ENSP00000377199.2:p.Ter660Lys
ENST00000544807.6:c.1744-735T>A	ENSP00000437513.2:n.1744-735T>A
ENST00000555000.5:c.1279-735T>A	ENSP00000450472.1:n.1279-735T>A
NM_000153.3:c.2056T>A	NP_000144.2:p.Ter686Lys
NM_001201401.1:c.1987T>A	NP_001188330.1:p.Ter663Lys
NM_001201402.1:c.1978T>A	NP_001188331.1:p.Ter660Lys
XM_011536618.1:c.1888T>A	XP_011534920.1:p.Ter630Lys
XM_011536618.2:c.1888T>A	XP_011534920.1:p.Ter630Lys
NM_000153.4:c.2056T>A MANE Select	NP_000144.2:p.Ter686Lys
NM_001201401.2:c.1987T>A	NP_001188330.1:p.Ter663Lys
NM_001201402.2:c.1978T>A	NP_001188331.1:p.Ter660Lys