Canonical Allele Identifier: CA2153352687

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87939912G= , CM000676.2:g.87939912G=	GRCh38
NC_000014.8:g.88406256G= , CM000676.1:g.88406256G=	GRCh37
NC_000014.7:g.87476009G=	NCBI36
NG_011853.2:g.58652C=
NG_011853.3:g.58652C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1904C= MANE Select	ENSP00000261304.2:p.Thr635=
ENST00000261304.6:c.1904C=	ENSP00000261304.2:p.Thr635=
ENST00000393568.8:c.1835C=	ENSP00000377198.4:p.Thr612=
ENST00000393569.6:c.1826C=	ENSP00000377199.2:p.Thr609=
ENST00000544807.6:c.1736C=	ENSP00000437513.2:p.Thr579=
ENST00000555000.5:c.1271C=	ENSP00000450472.1:p.Thr424=
ENST00000555179.1:c.440C=
NM_000153.3:c.1904C=	NP_000144.2:p.Thr635=
NM_001201401.1:c.1835C=	NP_001188330.1:p.Thr612=
NM_001201402.1:c.1826C=	NP_001188331.1:p.Thr609=
XM_011536618.1:c.1736C=	XP_011534920.1:p.Thr579=
XM_011536618.2:c.1736C=	XP_011534920.1:p.Thr579=
NM_000153.4:c.1904C= MANE Select	NP_000144.2:p.Thr635=
NM_001201401.2:c.1835C=	NP_001188330.1:p.Thr612=
NM_001201402.2:c.1826C=	NP_001188331.1:p.Thr609=