Canonical Allele Identifier: CA2201614961

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362250C= , CM000678.2:g.1362250C=	GRCh38
NC_000016.9:g.1412251C= , CM000678.1:g.1412251C=	GRCh37
NC_000016.8:g.1352252C=	NCBI36
NG_016985.1:g.15352C=
NG_033129.1:g.57455G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.555C=
ENST00000529110.2:c.540C=	ENSP00000435349.2:p.Ser180=
ENST00000529957.6:n.514C=
ENST00000683366.1:c.*188C=	ENSP00000507283.1:n.*188C=
ENST00000683887.1:c.504C=	ENSP00000506886.1:p.Ser168=
ENST00000684100.1:n.450C=
ENST00000684126.1:n.514C=
ENST00000684688.1:n.1081C=
ENST00000204679.9:c.456C= MANE Select	ENSP00000204679.4:p.Ser152=
ENST00000204679.8:c.456C=	ENSP00000204679.4:p.Ser152=
ENST00000527076.1:n.1472C=
ENST00000527168.5:n.492C=
ENST00000529110.1:c.523C=
ENST00000529957.5:n.555C=
NM_032520.4:c.456C=	NP_115909.1:p.Ser152=
XM_017023782.1:c.504C=	XP_016879271.1:p.Ser168=
XM_017023783.1:c.96C=	XP_016879272.1:p.Ser32=
NM_032520.5:c.456C= MANE Select	NP_115909.1:p.Ser152=