Canonical Allele Identifier: CA2201615151

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362460A= , CM000678.2:g.1362460A=	GRCh38
NC_000016.9:g.1412461A= , CM000678.1:g.1412461A=	GRCh37
NC_000016.8:g.1352462A=	NCBI36
NG_016985.1:g.15562A=
NG_033129.1:g.57245T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.634A=
ENST00000529110.2:c.619A=	ENSP00000435349.2:p.Thr207=
ENST00000529957.6:n.593A=
ENST00000683366.1:c.*267A=	ENSP00000507283.1:n.*267A=
ENST00000683887.1:c.583A=	ENSP00000506886.1:p.Thr195=
ENST00000684100.1:n.529A=
ENST00000684126.1:n.593A=
ENST00000684688.1:n.1160A=
ENST00000204679.9:c.535A= MANE Select	ENSP00000204679.4:p.Thr179=
ENST00000204679.8:c.535A=	ENSP00000204679.4:p.Thr179=
ENST00000527076.1:n.1682A=
ENST00000527168.5:n.702A=
ENST00000529957.5:n.634A=
NM_032520.4:c.535A=	NP_115909.1:p.Thr179=
XM_017023782.1:c.583A=	XP_016879271.1:p.Thr195=
XM_017023783.1:c.175A=	XP_016879272.1:p.Thr59=
NM_032520.5:c.535A= MANE Select	NP_115909.1:p.Thr179=