Canonical Allele Identifier: CA2201615239

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362581G= , CM000678.2:g.1362581G=	GRCh38
NC_000016.9:g.1412582G= , CM000678.1:g.1412582G=	GRCh37
NC_000016.8:g.1352583G=	NCBI36
NG_016985.1:g.15683G=
NG_033129.1:g.57124C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.709-30G=
ENST00000529110.2:c.694-30G=	ENSP00000435349.2:n.694-30G=
ENST00000529957.6:n.668-30G=
ENST00000683366.1:c.*342-30G=	ENSP00000507283.1:n.*342-30G=
ENST00000683887.1:c.658-30G=	ENSP00000506886.1:n.658-30G=
ENST00000684100.1:n.604-30G=
ENST00000684126.1:n.714G=
ENST00000684688.1:n.1235-30G=
ENST00000204679.9:c.610-30G= MANE Select	ENSP00000204679.4:n.610-30G=
ENST00000204679.8:c.610-30G=	ENSP00000204679.4:n.610-30G=
ENST00000527076.1:n.1803G=
ENST00000527168.5:n.777-30G=
ENST00000529957.5:n.709-30G=
NM_032520.4:c.610-30G=	NP_115909.1:n.610-30G=
XM_017023782.1:c.658-30G=	XP_016879271.1:n.658-30G=
XM_017023783.1:c.250-30G=	XP_016879272.1:n.250-30G=
NM_032520.5:c.610-30G= MANE Select	NP_115909.1:n.610-30G=