Canonical Allele Identifier: CA2201614418

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362024C= , CM000678.2:g.1362024C=	GRCh38
NC_000016.9:g.1412025C= , CM000678.1:g.1412025C=	GRCh37
NC_000016.8:g.1352026C=	NCBI36
NG_016985.1:g.15126C=
NG_033129.1:g.57681G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.417-14C=
ENST00000529110.2:c.402-14C=	ENSP00000435349.2:n.402-14C=
ENST00000529957.6:n.376-14C=
ENST00000683366.1:c.*50-14C=	ENSP00000507283.1:n.*50-14C=
ENST00000683887.1:c.366-14C=	ENSP00000506886.1:n.366-14C=
ENST00000684100.1:n.312-14C=
ENST00000684126.1:n.376-14C=
ENST00000684688.1:n.943-14C=
ENST00000204679.9:c.318-14C= MANE Select	ENSP00000204679.4:n.318-14C=
ENST00000204679.8:c.318-14C=	ENSP00000204679.4:n.318-14C=
ENST00000526820.5:c.*220-14C=	ENSP00000434413.1:n.*220-14C=
ENST00000527076.1:n.1334-14C=
ENST00000527168.5:n.354-14C=
ENST00000529110.1:c.385-14C=
ENST00000529957.5:n.417-14C=
NM_032520.4:c.318-14C=	NP_115909.1:n.318-14C=
XM_017023782.1:c.366-14C=	XP_016879271.1:n.366-14C=
XM_017023783.1:c.-43-14C=	XP_016879272.1:n.-43-14C=
NM_032520.5:c.318-14C= MANE Select	NP_115909.1:n.318-14C=