Canonical Allele Identifier: CA2153352667

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87939881C= , CM000676.2:g.87939881C=	GRCh38
NC_000014.8:g.88406225C= , CM000676.1:g.88406225C=	GRCh37
NC_000014.7:g.87475978C=	NCBI36
NG_011853.2:g.58683G=
NG_011853.3:g.58683G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1911+24G= MANE Select	ENSP00000261304.2:n.1911+24G=
ENST00000261304.6:c.1911+24G=	ENSP00000261304.2:n.1911+24G=
ENST00000393568.8:c.1842+24G=	ENSP00000377198.4:n.1842+24G=
ENST00000393569.6:c.1833+24G=	ENSP00000377199.2:n.1833+24G=
ENST00000544807.6:c.1743+24G=	ENSP00000437513.2:n.1743+24G=
ENST00000555000.5:c.1278+24G=	ENSP00000450472.1:n.1278+24G=
ENST00000555179.1:c.447+24G=
NM_000153.3:c.1911+24G=	NP_000144.2:n.1911+24G=
NM_001201401.1:c.1842+24G=	NP_001188330.1:n.1842+24G=
NM_001201402.1:c.1833+24G=	NP_001188331.1:n.1833+24G=
XM_011536618.1:c.1743+24G=	XP_011534920.1:n.1743+24G=
XM_011536618.2:c.1743+24G=	XP_011534920.1:n.1743+24G=
NM_000153.4:c.1911+24G= MANE Select	NP_000144.2:n.1911+24G=
NM_001201401.2:c.1842+24G=	NP_001188330.1:n.1842+24G=
NM_001201402.2:c.1833+24G=	NP_001188331.1:n.1833+24G=