Canonical Allele Identifier: CA2201614721

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362124A= , CM000678.2:g.1362124A=	GRCh38
NC_000016.9:g.1412125A= , CM000678.1:g.1412125A=	GRCh37
NC_000016.8:g.1352126A=	NCBI36
NG_016985.1:g.15226A=
NG_033129.1:g.57581T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.503A=
ENST00000529110.2:c.488A=	ENSP00000435349.2:p.Gln163=
ENST00000529957.6:n.462A=
ENST00000683366.1:c.*136A=	ENSP00000507283.1:n.*136A=
ENST00000683887.1:c.452A=	ENSP00000506886.1:p.Gln151=
ENST00000684100.1:n.398A=
ENST00000684126.1:n.462A=
ENST00000684688.1:n.1029A=
ENST00000204679.9:c.404A= MANE Select	ENSP00000204679.4:p.Gln135=
ENST00000204679.8:c.404A=	ENSP00000204679.4:p.Gln135=
ENST00000526820.5:c.*306A=	ENSP00000434413.1:n.*306A=
ENST00000527076.1:n.1420A=
ENST00000527168.5:n.440A=
ENST00000529110.1:c.471A=
ENST00000529957.5:n.503A=
NM_032520.4:c.404A=	NP_115909.1:p.Gln135=
XM_017023782.1:c.452A=	XP_016879271.1:p.Gln151=
XM_017023783.1:c.44A=	XP_016879272.1:p.Gln15=
NM_032520.5:c.404A= MANE Select	NP_115909.1:p.Gln135=