Canonical Allele Identifier: CA2201613922

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361825G= , CM000678.2:g.1361825G=	GRCh38
NC_000016.9:g.1411826G= , CM000678.1:g.1411826G=	GRCh37
NC_000016.8:g.1351827G=	NCBI36
NG_016985.1:g.14927G=
NG_033129.1:g.57880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.332+28G=
ENST00000529110.2:c.317+28G=	ENSP00000435349.2:n.317+28G=
ENST00000529957.6:n.291+28G=
ENST00000683366.1:c.179-47G=	ENSP00000507283.1:n.179-47G=
ENST00000683887.1:c.281+28G=	ENSP00000506886.1:n.281+28G=
ENST00000684100.1:n.181G=
ENST00000684126.1:n.291+28G=
ENST00000684688.1:n.858+28G=
ENST00000204679.9:c.233+28G= MANE Select	ENSP00000204679.4:n.233+28G=
ENST00000204679.8:c.233+28G=	ENSP00000204679.4:n.233+28G=
ENST00000526820.5:c.*135+28G=	ENSP00000434413.1:n.*135+28G=
ENST00000527076.1:n.1203G=
ENST00000527168.5:n.270-47G=
ENST00000529110.1:c.300+28G=
ENST00000529957.5:n.332+28G=
NM_032520.4:c.233+28G=	NP_115909.1:n.233+28G=
XM_017023782.1:c.281+28G=	XP_016879271.1:n.281+28G=
XM_017023783.1:c.-128+28G=	XP_016879272.1:n.-128+28G=
NM_032520.5:c.233+28G= MANE Select	NP_115909.1:n.233+28G=