Canonical Allele Identifier: CA2201614172

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361921A= , CM000678.2:g.1361921A=	GRCh38
NC_000016.9:g.1411922A= , CM000678.1:g.1411922A=	GRCh37
NC_000016.8:g.1351923A=	NCBI36
NG_016985.1:g.15023A=
NG_033129.1:g.57784T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.382A=
ENST00000529110.2:c.367A=	ENSP00000435349.2:p.Thr123=
ENST00000529957.6:n.341A=
ENST00000683366.1:c.*15A=	ENSP00000507283.1:n.*15A=
ENST00000683887.1:c.331A=	ENSP00000506886.1:p.Thr111=
ENST00000684100.1:n.277A=
ENST00000684126.1:n.341A=
ENST00000684688.1:n.908A=
ENST00000204679.9:c.283A= MANE Select	ENSP00000204679.4:p.Thr95=
ENST00000204679.8:c.283A=	ENSP00000204679.4:p.Thr95=
ENST00000526820.5:c.*185A=	ENSP00000434413.1:n.*185A=
ENST00000527076.1:n.1299A=
ENST00000527168.5:n.319A=
ENST00000529110.1:c.350A=
ENST00000529957.5:n.382A=
NM_032520.4:c.283A=	NP_115909.1:p.Thr95=
XM_017023782.1:c.331A=	XP_016879271.1:p.Thr111=
XM_017023783.1:c.-78A=	XP_016879272.1:n.-78A=
NM_032520.5:c.283A= MANE Select	NP_115909.1:p.Thr95=