Canonical Allele Identifier: CA2153381798

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976452G= , CM000676.2:g.87976452G=	GRCh38
NC_000014.8:g.88442796G= , CM000676.1:g.88442796G=	GRCh37
NC_000014.7:g.87512549G=	NCBI36
NG_011853.2:g.22112C=
NG_011853.3:g.22112C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.658C= MANE Select	ENSP00000261304.2:p.Arg220=
ENST00000261304.6:c.658C=	ENSP00000261304.2:p.Arg220=
ENST00000393568.8:c.589C=	ENSP00000377198.4:p.Arg197=
ENST00000393569.6:c.580C=	ENSP00000377199.2:p.Arg194=
ENST00000474294.6:n.648C=
ENST00000477716.3:n.413C=
ENST00000544807.6:c.490C=	ENSP00000437513.2:p.Arg164=
ENST00000554916.5:n.537C=
ENST00000555000.5:c.25C=	ENSP00000450472.1:p.Arg9=
ENST00000557316.5:c.*56C=	ENSP00000452314.1:n.*56C=
ENST00000622264.4:c.648C=
NM_000153.3:c.658C=	NP_000144.2:p.Arg220=
NM_001201401.1:c.589C=	NP_001188330.1:p.Arg197=
NM_001201402.1:c.580C=	NP_001188331.1:p.Arg194=
XM_011536618.1:c.490C=	XP_011534920.1:p.Arg164=
XM_011536618.2:c.490C=	XP_011534920.1:p.Arg164=
NM_000153.4:c.658C= MANE Select	NP_000144.2:p.Arg220=
NM_001201401.2:c.589C=	NP_001188330.1:p.Arg197=
NM_001201402.2:c.580C=	NP_001188331.1:p.Arg194=