Canonical Allele Identifier: CA2201615381

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362781T= , CM000678.2:g.1362781T=	GRCh38
NC_000016.9:g.1412782T= , CM000678.1:g.1412782T=	GRCh37
NC_000016.8:g.1352783T=	NCBI36
NG_016985.1:g.15883T=
NG_033129.1:g.56924A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.840+39T=
ENST00000529110.2:c.825+39T=	ENSP00000435349.2:n.825+39T=
ENST00000529957.6:n.799+39T=
ENST00000683366.1:c.*473+39T=	ENSP00000507283.1:n.*473+39T=
ENST00000683887.1:c.789+39T=	ENSP00000506886.1:n.789+39T=
ENST00000684100.1:n.735+39T=
ENST00000684126.1:n.875+39T=
ENST00000684688.1:n.1366+39T=
ENST00000204679.9:c.741+39T= MANE Select	ENSP00000204679.4:n.741+39T=
ENST00000204679.8:c.741+39T=	ENSP00000204679.4:n.741+39T=
ENST00000527076.1:n.1964+39T=
ENST00000527168.5:n.908+39T=
ENST00000529957.5:n.840+39T=
NM_032520.4:c.741+39T=	NP_115909.1:n.741+39T=
XM_017023782.1:c.789+39T=	XP_016879271.1:n.789+39T=
XM_017023783.1:c.381+39T=	XP_016879272.1:n.381+39T=
NM_032520.5:c.741+39T= MANE Select	NP_115909.1:n.741+39T=