Canonical Allele Identifier: CA2201614797

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362171T= , CM000678.2:g.1362171T=	GRCh38
NC_000016.9:g.1412172T= , CM000678.1:g.1412172T=	GRCh37
NC_000016.8:g.1352173T=	NCBI36
NG_016985.1:g.15273T=
NG_033129.1:g.57534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.511-35T=
ENST00000529110.2:c.496-35T=	ENSP00000435349.2:n.496-35T=
ENST00000529957.6:n.470-35T=
ENST00000683366.1:c.*144-35T=	ENSP00000507283.1:n.*144-35T=
ENST00000683887.1:c.460-35T=	ENSP00000506886.1:n.460-35T=
ENST00000684100.1:n.406-35T=
ENST00000684126.1:n.470-35T=
ENST00000684688.1:n.1037-35T=
ENST00000204679.9:c.412-35T= MANE Select	ENSP00000204679.4:n.412-35T=
ENST00000204679.8:c.412-35T=	ENSP00000204679.4:n.412-35T=
ENST00000527076.1:n.1428-35T=
ENST00000527168.5:n.448-35T=
ENST00000529110.1:c.479-35T=
ENST00000529957.5:n.511-35T=
NM_032520.4:c.412-35T=	NP_115909.1:n.412-35T=
XM_017023782.1:c.460-35T=	XP_016879271.1:n.460-35T=
XM_017023783.1:c.52-35T=	XP_016879272.1:n.52-35T=
NM_032520.5:c.412-35T= MANE Select	NP_115909.1:n.412-35T=