Canonical Allele Identifier: CA394187638

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412221T>A (hg19) ; chr16:g.1362220T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362220T>A , CM000678.2:g.1362220T>A	GRCh38
NC_000016.9:g.1412221T>A , CM000678.1:g.1412221T>A	GRCh37
NC_000016.8:g.1352222T>A	NCBI36
NG_016985.1:g.15322T>A
NG_033129.1:g.57485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.525T>A
ENST00000529110.2:c.510T>A	ENSP00000435349.2:p.Cys170Ter
ENST00000529957.6:n.484T>A
ENST00000683366.1:c.*158T>A	ENSP00000507283.1:n.*158T>A
ENST00000683887.1:c.474T>A	ENSP00000506886.1:p.Cys158Ter
ENST00000684100.1:n.420T>A
ENST00000684126.1:n.484T>A
ENST00000684688.1:n.1051T>A
ENST00000204679.9:c.426T>A MANE Select	ENSP00000204679.4:p.Cys142Ter
ENST00000204679.8:c.426T>A	ENSP00000204679.4:p.Cys142Ter
ENST00000527076.1:n.1442T>A
ENST00000527168.5:n.462T>A
ENST00000529110.1:c.493T>A
ENST00000529957.5:n.525T>A
NM_032520.4:c.426T>A	NP_115909.1:p.Cys142Ter
XM_017023782.1:c.474T>A	XP_016879271.1:p.Cys158Ter
XM_017023783.1:c.66T>A	XP_016879272.1:p.Cys22Ter
NM_032520.5:c.426T>A MANE Select	NP_115909.1:p.Cys142Ter