Canonical Allele Identifier: CA394187916

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412298T>A (hg19) ; chr16:g.1362297T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362297T>A , CM000678.2:g.1362297T>A	GRCh38
NC_000016.9:g.1412298T>A , CM000678.1:g.1412298T>A	GRCh37
NC_000016.8:g.1352299T>A	NCBI36
NG_016985.1:g.15399T>A
NG_033129.1:g.57408A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.602T>A
ENST00000529110.2:c.587T>A	ENSP00000435349.2:p.Val196Asp
ENST00000529957.6:n.561T>A
ENST00000683366.1:c.*235T>A	ENSP00000507283.1:n.*235T>A
ENST00000683887.1:c.551T>A	ENSP00000506886.1:p.Val184Asp
ENST00000684100.1:n.497T>A
ENST00000684126.1:n.561T>A
ENST00000684688.1:n.1128T>A
ENST00000204679.9:c.503T>A MANE Select	ENSP00000204679.4:p.Val168Asp
ENST00000204679.8:c.503T>A	ENSP00000204679.4:p.Val168Asp
ENST00000527076.1:n.1519T>A
ENST00000527168.5:n.539T>A
ENST00000529957.5:n.602T>A
NM_032520.4:c.503T>A	NP_115909.1:p.Val168Asp
XM_017023782.1:c.551T>A	XP_016879271.1:p.Val184Asp
XM_017023783.1:c.143T>A	XP_016879272.1:p.Val48Asp
NM_032520.5:c.503T>A MANE Select	NP_115909.1:p.Val168Asp