Canonical Allele Identifier: CA2153381738

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87976326A= , CM000676.2:g.87976326A=	GRCh38
NC_000014.8:g.88442670A= , CM000676.1:g.88442670A=	GRCh37
NC_000014.7:g.87512423A=	NCBI36
NG_011853.2:g.22238T=
NG_011853.3:g.22238T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.752+32T= MANE Select	ENSP00000261304.2:n.752+32T=
ENST00000261304.6:c.752+32T=	ENSP00000261304.2:n.752+32T=
ENST00000393568.8:c.683+32T=	ENSP00000377198.4:n.683+32T=
ENST00000393569.6:c.674+32T=	ENSP00000377199.2:n.674+32T=
ENST00000474294.6:n.742+32T=
ENST00000477716.3:n.507+32T=
ENST00000544807.6:c.584+32T=	ENSP00000437513.2:n.584+32T=
ENST00000555000.5:c.119+32T=	ENSP00000450472.1:n.119+32T=
ENST00000557316.5:c.*150+32T=	ENSP00000452314.1:n.*150+32T=
ENST00000622264.4:c.742+32T=
NM_000153.3:c.752+32T=	NP_000144.2:n.752+32T=
NM_001201401.1:c.683+32T=	NP_001188330.1:n.683+32T=
NM_001201402.1:c.674+32T=	NP_001188331.1:n.674+32T=
XM_011536618.1:c.584+32T=	XP_011534920.1:n.584+32T=
XM_011536618.2:c.584+32T=	XP_011534920.1:n.584+32T=
NM_000153.4:c.752+32T= MANE Select	NP_000144.2:n.752+32T=
NM_001201401.2:c.683+32T=	NP_001188330.1:n.683+32T=
NM_001201402.2:c.674+32T=	NP_001188331.1:n.674+32T=