Canonical Allele Identifier: CA2201614114

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361898A= , CM000678.2:g.1361898A=	GRCh38
NC_000016.9:g.1411899A= , CM000678.1:g.1411899A=	GRCh37
NC_000016.8:g.1351900A=	NCBI36
NG_016985.1:g.15000A=
NG_033129.1:g.57807T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.359A=
ENST00000529110.2:c.344A=	ENSP00000435349.2:p.His115=
ENST00000529957.6:n.318A=
ENST00000683366.1:c.205A=	ENSP00000507283.1:p.Thr69=
ENST00000683887.1:c.308A=	ENSP00000506886.1:p.His103=
ENST00000684100.1:n.254A=
ENST00000684126.1:n.318A=
ENST00000684688.1:n.885A=
ENST00000204679.9:c.260A= MANE Select	ENSP00000204679.4:p.His87=
ENST00000204679.8:c.260A=	ENSP00000204679.4:p.His87=
ENST00000526820.5:c.*162A=	ENSP00000434413.1:n.*162A=
ENST00000527076.1:n.1276A=
ENST00000527168.5:n.296A=
ENST00000529110.1:c.327A=
ENST00000529957.5:n.359A=
NM_032520.4:c.260A=	NP_115909.1:p.His87=
XM_017023782.1:c.308A=	XP_016879271.1:p.His103=
XM_017023783.1:c.-101A=	XP_016879272.1:n.-101A=
NM_032520.5:c.260A= MANE Select	NP_115909.1:p.His87=