Canonical Allele Identifier: CA394188476

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362659A>T , CM000678.2:g.1362659A>T	GRCh38
NC_000016.9:g.1412660A>T , CM000678.1:g.1412660A>T	GRCh37
NC_000016.8:g.1352661A>T	NCBI36
NG_016985.1:g.15761A>T
NG_033129.1:g.57046T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032520.5:c.658A>T MANE Select	NP_115909.1:p.Lys220Ter
ENST00000204679.9:c.658A>T MANE Select	ENSP00000204679.4:p.Lys220Ter
NM_032520.4:c.658A>T	NP_115909.1:p.Lys220Ter
ENST00000204679.8:c.658A>T	ENSP00000204679.4:p.Lys220Ter
ENST00000527076.1:n.1881A>T
ENST00000527168.5:n.825A>T
ENST00000527168.6:n.757A>T
ENST00000529110.2:c.742A>T	ENSP00000435349.2:p.Lys248Ter
ENST00000529957.5:n.757A>T
ENST00000529957.6:n.716A>T
ENST00000683366.1:c.*390A>T	ENSP00000507283.1:n.*390A>T
ENST00000683887.1:c.706A>T	ENSP00000506886.1:p.Lys236Ter
ENST00000684100.1:n.652A>T
ENST00000684126.1:n.792A>T
ENST00000684688.1:n.1283A>T
XM_017023782.1:c.706A>T	XP_016879271.1:p.Lys236Ter
XM_017023783.1:c.298A>T	XP_016879272.1:p.Lys100Ter