Canonical Allele Identifier: CA394187588

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412210G>T (hg19) ; chr16:g.1362209G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362209G>T , CM000678.2:g.1362209G>T	GRCh38
NC_000016.9:g.1412210G>T , CM000678.1:g.1412210G>T	GRCh37
NC_000016.8:g.1352211G>T	NCBI36
NG_016985.1:g.15311G>T
NG_033129.1:g.57496C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.514G>T
ENST00000529110.2:c.499G>T	ENSP00000435349.2:p.Glu167Ter
ENST00000529957.6:n.473G>T
ENST00000683366.1:c.*147G>T	ENSP00000507283.1:n.*147G>T
ENST00000683887.1:c.463G>T	ENSP00000506886.1:p.Glu155Ter
ENST00000684100.1:n.409G>T
ENST00000684126.1:n.473G>T
ENST00000684688.1:n.1040G>T
ENST00000204679.9:c.415G>T MANE Select	ENSP00000204679.4:p.Glu139Ter
ENST00000204679.8:c.415G>T	ENSP00000204679.4:p.Glu139Ter
ENST00000527076.1:n.1431G>T
ENST00000527168.5:n.451G>T
ENST00000529110.1:c.482G>T
ENST00000529957.5:n.514G>T
NM_032520.4:c.415G>T	NP_115909.1:p.Glu139Ter
XM_017023782.1:c.463G>T	XP_016879271.1:p.Glu155Ter
XM_017023783.1:c.55G>T	XP_016879272.1:p.Glu19Ter
NM_032520.5:c.415G>T MANE Select	NP_115909.1:p.Glu139Ter