Canonical Allele Identifier: CA2201613567

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361606T= , CM000678.2:g.1361606T=	GRCh38
NC_000016.9:g.1411607T= , CM000678.1:g.1411607T=	GRCh37
NC_000016.8:g.1351608T=	NCBI36
NG_016985.1:g.14708T=
NG_033129.1:g.58099A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.278-137T=
ENST00000529110.2:c.263-137T=	ENSP00000435349.2:n.263-137T=
ENST00000529957.6:n.237-137T=
ENST00000683366.1:c.179-266T=	ENSP00000507283.1:n.179-266T=
ENST00000683887.1:c.179-89T=	ENSP00000506886.1:n.179-89T=
ENST00000684126.1:n.237-137T=
ENST00000684688.1:n.667T=
ENST00000204679.9:c.179-137T= MANE Select	ENSP00000204679.4:n.179-137T=
ENST00000204679.8:c.179-137T=	ENSP00000204679.4:n.179-137T=
ENST00000526820.5:c.*81-137T=	ENSP00000434413.1:n.*81-137T=
ENST00000527076.1:n.984T=
ENST00000527168.5:n.270-266T=
ENST00000529110.1:c.246-137T=
ENST00000529957.5:n.278-137T=
NM_032520.4:c.179-137T=	NP_115909.1:n.179-137T=
XM_017023782.1:c.179-89T=	XP_016879271.1:n.179-89T=
XM_017023783.1:c.-182-137T=	XP_016879272.1:n.-182-137T=
NM_032520.5:c.179-137T= MANE Select	NP_115909.1:n.179-137T=