Canonical Allele Identifier: CA2201614989

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362260A= , CM000678.2:g.1362260A=	GRCh38
NC_000016.9:g.1412261A= , CM000678.1:g.1412261A=	GRCh37
NC_000016.8:g.1352262A=	NCBI36
NG_016985.1:g.15362A=
NG_033129.1:g.57445T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.565A=
ENST00000529110.2:c.550A=	ENSP00000435349.2:p.Thr184=
ENST00000529957.6:n.524A=
ENST00000683366.1:c.*198A=	ENSP00000507283.1:n.*198A=
ENST00000683887.1:c.514A=	ENSP00000506886.1:p.Thr172=
ENST00000684100.1:n.460A=
ENST00000684126.1:n.524A=
ENST00000684688.1:n.1091A=
ENST00000204679.9:c.466A= MANE Select	ENSP00000204679.4:p.Thr156=
ENST00000204679.8:c.466A=	ENSP00000204679.4:p.Thr156=
ENST00000527076.1:n.1482A=
ENST00000527168.5:n.502A=
ENST00000529110.1:c.533A=
ENST00000529957.5:n.565A=
NM_032520.4:c.466A=	NP_115909.1:p.Thr156=
XM_017023782.1:c.514A=	XP_016879271.1:p.Thr172=
XM_017023783.1:c.106A=	XP_016879272.1:p.Thr36=
NM_032520.5:c.466A= MANE Select	NP_115909.1:p.Thr156=