Canonical Allele Identifier: CA394188296

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412513C>A (hg19) ; chr16:g.1362512C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362512C>A , CM000678.2:g.1362512C>A	GRCh38
NC_000016.9:g.1412513C>A , CM000678.1:g.1412513C>A	GRCh37
NC_000016.8:g.1352514C>A	NCBI36
NG_016985.1:g.15614C>A
NG_033129.1:g.57193G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.686C>A
ENST00000529110.2:c.671C>A	ENSP00000435349.2:p.Ala224Asp
ENST00000529957.6:n.645C>A
ENST00000683366.1:c.*319C>A	ENSP00000507283.1:n.*319C>A
ENST00000683887.1:c.635C>A	ENSP00000506886.1:p.Ala212Asp
ENST00000684100.1:n.581C>A
ENST00000684126.1:n.645C>A
ENST00000684688.1:n.1212C>A
ENST00000204679.9:c.587C>A MANE Select	ENSP00000204679.4:p.Ala196Asp
ENST00000204679.8:c.587C>A	ENSP00000204679.4:p.Ala196Asp
ENST00000527076.1:n.1734C>A
ENST00000527168.5:n.754C>A
ENST00000529957.5:n.686C>A
NM_032520.4:c.587C>A	NP_115909.1:p.Ala196Asp
XM_017023782.1:c.635C>A	XP_016879271.1:p.Ala212Asp
XM_017023783.1:c.227C>A	XP_016879272.1:p.Ala76Asp
NM_032520.5:c.587C>A MANE Select	NP_115909.1:p.Ala196Asp