Canonical Allele Identifier: CA2201615241

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362583G= , CM000678.2:g.1362583G=	GRCh38
NC_000016.9:g.1412584G= , CM000678.1:g.1412584G=	GRCh37
NC_000016.8:g.1352585G=	NCBI36
NG_016985.1:g.15685G=
NG_033129.1:g.57122C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.709-28G=
ENST00000529110.2:c.694-28G=	ENSP00000435349.2:n.694-28G=
ENST00000529957.6:n.668-28G=
ENST00000683366.1:c.*342-28G=	ENSP00000507283.1:n.*342-28G=
ENST00000683887.1:c.658-28G=	ENSP00000506886.1:n.658-28G=
ENST00000684100.1:n.604-28G=
ENST00000684126.1:n.716G=
ENST00000684688.1:n.1235-28G=
ENST00000204679.9:c.610-28G= MANE Select	ENSP00000204679.4:n.610-28G=
ENST00000204679.8:c.610-28G=	ENSP00000204679.4:n.610-28G=
ENST00000527076.1:n.1805G=
ENST00000527168.5:n.777-28G=
ENST00000529957.5:n.709-28G=
NM_032520.4:c.610-28G=	NP_115909.1:n.610-28G=
XM_017023782.1:c.658-28G=	XP_016879271.1:n.658-28G=
XM_017023783.1:c.250-28G=	XP_016879272.1:n.250-28G=
NM_032520.5:c.610-28G= MANE Select	NP_115909.1:n.610-28G=