Canonical Allele Identifier: CA2739278035

Gene: GALC

Linked Data

• ClinVar Variation Id: 2860299
• ClinVar RCV Id: RCV003609068

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988448T>A , CM000676.2:g.87988448T>A	GRCh38
NC_000014.8:g.88454792T>A , CM000676.1:g.88454792T>A	GRCh37
NC_000014.7:g.87524545T>A	NCBI36
NG_011853.2:g.10116A>T
NG_011853.3:g.10116A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.264+7A>T MANE Select	ENSP00000261304.2:n.264+7A>T
ENST00000261304.6:c.264+7A>T	ENSP00000261304.2:n.264+7A>T
ENST00000393568.8:c.196-241A>T	ENSP00000377198.4:n.196-241A>T
ENST00000393569.6:c.186+7A>T	ENSP00000377199.2:n.186+7A>T
ENST00000474294.6:n.254+7A>T
ENST00000544807.6:c.96+7A>T	ENSP00000437513.2:n.96+7A>T
ENST00000554372.5:c.264+7A>T	ENSP00000451884.1:n.264+7A>T
ENST00000554916.5:n.143+7A>T
ENST00000555956.1:n.69+7A>T
ENST00000556879.5:c.324+7A>T	ENSP00000452208.1:n.324+7A>T
ENST00000557316.5:c.264+7A>T	ENSP00000452314.1:n.264+7A>T
ENST00000622264.4:c.254+7A>T
NM_000153.3:c.264+7A>T	NP_000144.2:n.264+7A>T
NM_001201401.1:c.196-241A>T	NP_001188330.1:n.196-241A>T
NM_001201402.1:c.186+7A>T	NP_001188331.1:n.186+7A>T
XM_011536618.1:c.96+7A>T	XP_011534920.1:n.96+7A>T
XM_011536618.2:c.96+7A>T	XP_011534920.1:n.96+7A>T
NM_000153.4:c.264+7A>T MANE Select	NP_000144.2:n.264+7A>T
NM_001201401.2:c.196-241A>T	NP_001188330.1:n.196-241A>T
NM_001201402.2:c.186+7A>T	NP_001188331.1:n.186+7A>T