Canonical Allele Identifier: CA2153358480

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947437A= , CM000676.2:g.87947437A=	GRCh38
NC_000014.8:g.88413781A= , CM000676.1:g.88413781A=	GRCh37
NC_000014.7:g.87483534A=	NCBI36
NG_011853.2:g.51127T=
NG_011853.3:g.51127T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.1489+291T= MANE Select	ENSP00000261304.2:n.1489+291T=
ENST00000261304.6:c.1489+291T=	ENSP00000261304.2:n.1489+291T=
ENST00000393568.8:c.1420+291T=	ENSP00000377198.4:n.1420+291T=
ENST00000393569.6:c.1411+291T=	ENSP00000377199.2:n.1411+291T=
ENST00000544807.6:c.1321+291T=	ENSP00000437513.2:n.1321+291T=
ENST00000555000.5:c.856+291T=	ENSP00000450472.1:n.856+291T=
ENST00000555179.1:c.206+291T=
ENST00000557316.5:c.*887+291T=	ENSP00000452314.1:n.*887+291T=
NM_000153.3:c.1489+291T=	NP_000144.2:n.1489+291T=
NM_001201401.1:c.1420+291T=	NP_001188330.1:n.1420+291T=
NM_001201402.1:c.1411+291T=	NP_001188331.1:n.1411+291T=
XM_011536618.1:c.1321+291T=	XP_011534920.1:n.1321+291T=
XM_011536618.2:c.1321+291T=	XP_011534920.1:n.1321+291T=
NM_000153.4:c.1489+291T= MANE Select	NP_000144.2:n.1489+291T=
NM_001201401.2:c.1420+291T=	NP_001188330.1:n.1420+291T=
NM_001201402.2:c.1411+291T=	NP_001188331.1:n.1411+291T=