Canonical Allele Identifier: CA2201613606

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361632A= , CM000678.2:g.1361632A=	GRCh38
NC_000016.9:g.1411633A= , CM000678.1:g.1411633A=	GRCh37
NC_000016.8:g.1351634A=	NCBI36
NG_016985.1:g.14734A=
NG_033129.1:g.58073T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.278-111A=
ENST00000529110.2:c.263-111A=	ENSP00000435349.2:n.263-111A=
ENST00000529957.6:n.237-111A=
ENST00000683366.1:c.179-240A=	ENSP00000507283.1:n.179-240A=
ENST00000683887.1:c.179-63A=	ENSP00000506886.1:n.179-63A=
ENST00000684126.1:n.237-111A=
ENST00000684688.1:n.693A=
ENST00000204679.9:c.179-111A= MANE Select	ENSP00000204679.4:n.179-111A=
ENST00000204679.8:c.179-111A=	ENSP00000204679.4:n.179-111A=
ENST00000526820.5:c.*81-111A=	ENSP00000434413.1:n.*81-111A=
ENST00000527076.1:n.1010A=
ENST00000527168.5:n.270-240A=
ENST00000529110.1:c.246-111A=
ENST00000529957.5:n.278-111A=
NM_032520.4:c.179-111A=	NP_115909.1:n.179-111A=
XM_017023782.1:c.179-63A=	XP_016879271.1:n.179-63A=
XM_017023783.1:c.-182-111A=	XP_016879272.1:n.-182-111A=
NM_032520.5:c.179-111A= MANE Select	NP_115909.1:n.179-111A=