Canonical Allele Identifier: CA2201615232

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362570G= , CM000678.2:g.1362570G=	GRCh38
NC_000016.9:g.1412571G= , CM000678.1:g.1412571G=	GRCh37
NC_000016.8:g.1352572G=	NCBI36
NG_016985.1:g.15672G=
NG_033129.1:g.57135C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.708+36G=
ENST00000529110.2:c.693+36G=	ENSP00000435349.2:n.693+36G=
ENST00000529957.6:n.667+36G=
ENST00000683366.1:c.*341+36G=	ENSP00000507283.1:n.*341+36G=
ENST00000683887.1:c.657+36G=	ENSP00000506886.1:n.657+36G=
ENST00000684100.1:n.603+36G=
ENST00000684126.1:n.703G=
ENST00000684688.1:n.1234+36G=
ENST00000204679.9:c.609+36G= MANE Select	ENSP00000204679.4:n.609+36G=
ENST00000204679.8:c.609+36G=	ENSP00000204679.4:n.609+36G=
ENST00000527076.1:n.1792G=
ENST00000527168.5:n.776+36G=
ENST00000529957.5:n.708+36G=
NM_032520.4:c.609+36G=	NP_115909.1:n.609+36G=
XM_017023782.1:c.657+36G=	XP_016879271.1:n.657+36G=
XM_017023783.1:c.249+36G=	XP_016879272.1:n.249+36G=
NM_032520.5:c.609+36G= MANE Select	NP_115909.1:n.609+36G=