Canonical Allele Identifier: CA394188798

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412893A>G (hg19) ; chr16:g.1362892A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362892A>G , CM000678.2:g.1362892A>G	GRCh38
NC_000016.9:g.1412893A>G , CM000678.1:g.1412893A>G	GRCh37
NC_000016.8:g.1352894A>G	NCBI36
NG_016985.1:g.15994A>G
NG_033129.1:g.56813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.908A>G
ENST00000529110.2:c.893A>G	ENSP00000435349.2:p.Tyr298Cys
ENST00000529957.6:n.867A>G
ENST00000683366.1:c.*541A>G	ENSP00000507283.1:n.*541A>G
ENST00000683887.1:c.857A>G	ENSP00000506886.1:p.Tyr286Cys
ENST00000684100.1:n.803A>G
ENST00000684126.1:n.943A>G
ENST00000684688.1:n.1434A>G
ENST00000204679.9:c.809A>G MANE Select	ENSP00000204679.4:p.Tyr270Cys
ENST00000204679.8:c.809A>G	ENSP00000204679.4:p.Tyr270Cys
ENST00000527076.1:n.2032A>G
ENST00000527168.5:n.976A>G
ENST00000529957.5:n.908A>G
NM_032520.4:c.809A>G	NP_115909.1:p.Tyr270Cys
XM_017023782.1:c.857A>G	XP_016879271.1:p.Tyr286Cys
XM_017023783.1:c.449A>G	XP_016879272.1:p.Tyr150Cys
NM_032520.5:c.809A>G MANE Select	NP_115909.1:p.Tyr270Cys