Canonical Allele Identifier: CA2153350293

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934691G= , CM000676.2:g.87934691G=	GRCh38
NC_000014.8:g.88401035G= , CM000676.1:g.88401035G=	GRCh37
NC_000014.7:g.87470788G=	NCBI36
NG_011853.2:g.63873C=
NG_011853.3:g.63873C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.*41C= MANE Select	ENSP00000261304.2:n.*41C=
ENST00000261304.6:c.*41C=	ENSP00000261304.2:n.*41C=
ENST00000393568.8:c.*41C=	ENSP00000377198.4:n.*41C=
ENST00000393569.6:c.*41C=	ENSP00000377199.2:n.*41C=
ENST00000544807.6:c.1744-692C=	ENSP00000437513.2:n.1744-692C=
ENST00000555000.5:c.1279-692C=	ENSP00000450472.1:n.1279-692C=
NM_000153.3:c.*41C=	NP_000144.2:n.*41C=
NM_001201401.1:c.*41C=	NP_001188330.1:n.*41C=
NM_001201402.1:c.*41C=	NP_001188331.1:n.*41C=
XM_011536618.1:c.*41C=	XP_011534920.1:n.*41C=
XM_011536618.2:c.*41C=	XP_011534920.1:n.*41C=
NM_000153.4:c.*41C= MANE Select	NP_000144.2:n.*41C=
NM_001201401.2:c.*41C=	NP_001188330.1:n.*41C=
NM_001201402.2:c.*41C=	NP_001188331.1:n.*41C=