Canonical Allele Identifier: CA2153387451

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87988493C= , CM000676.2:g.87988493C=	GRCh38
NC_000014.8:g.88454837C= , CM000676.1:g.88454837C=	GRCh37
NC_000014.7:g.87524590C=	NCBI36
NG_011853.2:g.10071G=
NG_011853.3:g.10071G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.226G= MANE Select	ENSP00000261304.2:p.Glu76=
ENST00000261304.6:c.226G=	ENSP00000261304.2:p.Glu76=
ENST00000393568.8:c.196-286G=	ENSP00000377198.4:n.196-286G=
ENST00000393569.6:c.148G=	ENSP00000377199.2:p.Glu50=
ENST00000474294.6:n.216G=
ENST00000544807.6:c.58G=	ENSP00000437513.2:p.Glu20=
ENST00000554372.5:c.226G=	ENSP00000451884.1:p.Glu76=
ENST00000554916.5:n.105G=
ENST00000555956.1:n.31G=
ENST00000556879.5:c.286G=	ENSP00000452208.1:n.286G=
ENST00000557316.5:c.226G=	ENSP00000452314.1:p.Glu76=
ENST00000622264.4:c.216G=
NM_000153.3:c.226G=	NP_000144.2:p.Glu76=
NM_001201401.1:c.196-286G=	NP_001188330.1:n.196-286G=
NM_001201402.1:c.148G=	NP_001188331.1:p.Glu50=
XM_011536618.1:c.58G=	XP_011534920.1:p.Glu20=
XM_011536618.2:c.58G=	XP_011534920.1:p.Glu20=
NM_000153.4:c.226G= MANE Select	NP_000144.2:p.Glu76=
NM_001201401.2:c.196-286G=	NP_001188330.1:n.196-286G=
NM_001201402.2:c.148G=	NP_001188331.1:p.Glu50=