Canonical Allele Identifier: CA394188762

Gene: GNPTG

Linked Data

• dbSNP Id: rs2141865402
• MyVariant Identifiers: chr16:g.1412874A>T (hg19) ; chr16:g.1362873A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362873A>T , CM000678.2:g.1362873A>T	GRCh38
NC_000016.9:g.1412874A>T , CM000678.1:g.1412874A>T	GRCh37
NC_000016.8:g.1352875A>T	NCBI36
NG_016985.1:g.15975A>T
NG_033129.1:g.56832T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.889A>T
ENST00000529110.2:c.874A>T	ENSP00000435349.2:p.Thr292Ser
ENST00000529957.6:n.848A>T
ENST00000683366.1:c.*522A>T	ENSP00000507283.1:n.*522A>T
ENST00000683887.1:c.838A>T	ENSP00000506886.1:p.Thr280Ser
ENST00000684100.1:n.784A>T
ENST00000684126.1:n.924A>T
ENST00000684688.1:n.1415A>T
ENST00000204679.9:c.790A>T MANE Select	ENSP00000204679.4:p.Thr264Ser
ENST00000204679.8:c.790A>T	ENSP00000204679.4:p.Thr264Ser
ENST00000527076.1:n.2013A>T
ENST00000527168.5:n.957A>T
ENST00000529957.5:n.889A>T
NM_032520.4:c.790A>T	NP_115909.1:p.Thr264Ser
XM_017023782.1:c.838A>T	XP_016879271.1:p.Thr280Ser
XM_017023783.1:c.430A>T	XP_016879272.1:p.Thr144Ser
NM_032520.5:c.790A>T MANE Select	NP_115909.1:p.Thr264Ser