Canonical Allele Identifier: CA2153381649

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976137G= , CM000676.2:g.87976137G=	GRCh38
NC_000014.8:g.88442481G= , CM000676.1:g.88442481G=	GRCh37
NC_000014.7:g.87512234G=	NCBI36
NG_011853.2:g.22427C=
NG_011853.3:g.22427C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.752+221C= MANE Select	ENSP00000261304.2:n.752+221C=
ENST00000261304.6:c.752+221C=	ENSP00000261304.2:n.752+221C=
ENST00000393568.8:c.683+221C=	ENSP00000377198.4:n.683+221C=
ENST00000393569.6:c.674+221C=	ENSP00000377199.2:n.674+221C=
ENST00000474294.6:n.742+221C=
ENST00000477716.3:n.507+221C=
ENST00000544807.6:c.584+221C=	ENSP00000437513.2:n.584+221C=
ENST00000555000.5:c.119+221C=	ENSP00000450472.1:n.119+221C=
ENST00000557316.5:c.*150+221C=	ENSP00000452314.1:n.*150+221C=
ENST00000622264.4:c.742+221C=
NM_000153.3:c.752+221C=	NP_000144.2:n.752+221C=
NM_001201401.1:c.683+221C=	NP_001188330.1:n.683+221C=
NM_001201402.1:c.674+221C=	NP_001188331.1:n.674+221C=
XM_011536618.1:c.584+221C=	XP_011534920.1:n.584+221C=
XM_011536618.2:c.584+221C=	XP_011534920.1:n.584+221C=
NM_000153.4:c.752+221C= MANE Select	NP_000144.2:n.752+221C=
NM_001201401.2:c.683+221C=	NP_001188330.1:n.683+221C=
NM_001201402.2:c.674+221C=	NP_001188331.1:n.674+221C=