Canonical Allele Identifier: CA394188741

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412863A>G (hg19) ; chr16:g.1362862A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362862A>G , CM000678.2:g.1362862A>G	GRCh38
NC_000016.9:g.1412863A>G , CM000678.1:g.1412863A>G	GRCh37
NC_000016.8:g.1352864A>G	NCBI36
NG_016985.1:g.15964A>G
NG_033129.1:g.56843T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.878A>G
ENST00000529110.2:c.863A>G	ENSP00000435349.2:p.Lys288Arg
ENST00000529957.6:n.837A>G
ENST00000683366.1:c.*511A>G	ENSP00000507283.1:n.*511A>G
ENST00000683887.1:c.827A>G	ENSP00000506886.1:p.Lys276Arg
ENST00000684100.1:n.773A>G
ENST00000684126.1:n.913A>G
ENST00000684688.1:n.1404A>G
ENST00000204679.9:c.779A>G MANE Select	ENSP00000204679.4:p.Lys260Arg
ENST00000204679.8:c.779A>G	ENSP00000204679.4:p.Lys260Arg
ENST00000527076.1:n.2002A>G
ENST00000527168.5:n.946A>G
ENST00000529957.5:n.878A>G
NM_032520.4:c.779A>G	NP_115909.1:p.Lys260Arg
XM_017023782.1:c.827A>G	XP_016879271.1:p.Lys276Arg
XM_017023783.1:c.419A>G	XP_016879272.1:p.Lys140Arg
NM_032520.5:c.779A>G MANE Select	NP_115909.1:p.Lys260Arg