Canonical Allele Identifier: CA2201615231

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362569T= , CM000678.2:g.1362569T=	GRCh38
NC_000016.9:g.1412570T= , CM000678.1:g.1412570T=	GRCh37
NC_000016.8:g.1352571T=	NCBI36
NG_016985.1:g.15671T=
NG_033129.1:g.57136A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.708+35T=
ENST00000529110.2:c.693+35T=	ENSP00000435349.2:n.693+35T=
ENST00000529957.6:n.667+35T=
ENST00000683366.1:c.*341+35T=	ENSP00000507283.1:n.*341+35T=
ENST00000683887.1:c.657+35T=	ENSP00000506886.1:n.657+35T=
ENST00000684100.1:n.603+35T=
ENST00000684126.1:n.702T=
ENST00000684688.1:n.1234+35T=
ENST00000204679.9:c.609+35T= MANE Select	ENSP00000204679.4:n.609+35T=
ENST00000204679.8:c.609+35T=	ENSP00000204679.4:n.609+35T=
ENST00000527076.1:n.1791T=
ENST00000527168.5:n.776+35T=
ENST00000529957.5:n.708+35T=
NM_032520.4:c.609+35T=	NP_115909.1:n.609+35T=
XM_017023782.1:c.657+35T=	XP_016879271.1:n.657+35T=
XM_017023783.1:c.249+35T=	XP_016879272.1:n.249+35T=
NM_032520.5:c.609+35T= MANE Select	NP_115909.1:n.609+35T=