Canonical Allele Identifier: CA394188664

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412827C>A (hg19) ; chr16:g.1362826C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362826C>A , CM000678.2:g.1362826C>A	GRCh38
NC_000016.9:g.1412827C>A , CM000678.1:g.1412827C>A	GRCh37
NC_000016.8:g.1352828C>A	NCBI36
NG_016985.1:g.15928C>A
NG_033129.1:g.56879G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.842C>A
ENST00000529110.2:c.827C>A	ENSP00000435349.2:p.Ala276Asp
ENST00000529957.6:n.801C>A
ENST00000683366.1:c.*475C>A	ENSP00000507283.1:n.*475C>A
ENST00000683887.1:c.791C>A	ENSP00000506886.1:p.Ala264Asp
ENST00000684100.1:n.737C>A
ENST00000684126.1:n.877C>A
ENST00000684688.1:n.1368C>A
ENST00000204679.9:c.743C>A MANE Select	ENSP00000204679.4:p.Ala248Asp
ENST00000204679.8:c.743C>A	ENSP00000204679.4:p.Ala248Asp
ENST00000527076.1:n.1966C>A
ENST00000527168.5:n.910C>A
ENST00000529957.5:n.842C>A
NM_032520.4:c.743C>A	NP_115909.1:p.Ala248Asp
XM_017023782.1:c.791C>A	XP_016879271.1:p.Ala264Asp
XM_017023783.1:c.383C>A	XP_016879272.1:p.Ala128Asp
NM_032520.5:c.743C>A MANE Select	NP_115909.1:p.Ala248Asp