Canonical Allele Identifier: CA2201613671

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361701T= , CM000678.2:g.1361701T=	GRCh38
NC_000016.9:g.1411702T= , CM000678.1:g.1411702T=	GRCh37
NC_000016.8:g.1351703T=	NCBI36
NG_016985.1:g.14803T=
NG_033129.1:g.58004A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.278-42T=
ENST00000529110.2:c.263-42T=	ENSP00000435349.2:n.263-42T=
ENST00000529957.6:n.237-42T=
ENST00000683366.1:c.179-171T=	ENSP00000507283.1:n.179-171T=
ENST00000683887.1:c.185T=	ENSP00000506886.1:p.Phe62=
ENST00000684100.1:n.57T=
ENST00000684126.1:n.237-42T=
ENST00000684688.1:n.762T=
ENST00000204679.9:c.179-42T= MANE Select	ENSP00000204679.4:n.179-42T=
ENST00000204679.8:c.179-42T=	ENSP00000204679.4:n.179-42T=
ENST00000526820.5:c.*81-42T=	ENSP00000434413.1:n.*81-42T=
ENST00000527076.1:n.1079T=
ENST00000527168.5:n.270-171T=
ENST00000529110.1:c.246-42T=
ENST00000529957.5:n.278-42T=
NM_032520.4:c.179-42T=	NP_115909.1:n.179-42T=
XM_017023782.1:c.185T=	XP_016879271.1:p.Phe62=
XM_017023783.1:c.-182-42T=	XP_016879272.1:n.-182-42T=
NM_032520.5:c.179-42T= MANE Select	NP_115909.1:n.179-42T=