Canonical Allele Identifier: CA394187946

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412312G>T (hg19) ; chr16:g.1362311G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362311G>T , CM000678.2:g.1362311G>T	GRCh38
NC_000016.9:g.1412312G>T , CM000678.1:g.1412312G>T	GRCh37
NC_000016.8:g.1352313G>T	NCBI36
NG_016985.1:g.15413G>T
NG_033129.1:g.57394C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.616G>T
ENST00000529110.2:c.601G>T	ENSP00000435349.2:p.Ala201Ser
ENST00000529957.6:n.575G>T
ENST00000683366.1:c.*249G>T	ENSP00000507283.1:n.*249G>T
ENST00000683887.1:c.565G>T	ENSP00000506886.1:p.Ala189Ser
ENST00000684100.1:n.511G>T
ENST00000684126.1:n.575G>T
ENST00000684688.1:n.1142G>T
ENST00000204679.9:c.517G>T MANE Select	ENSP00000204679.4:p.Ala173Ser
ENST00000204679.8:c.517G>T	ENSP00000204679.4:p.Ala173Ser
ENST00000527076.1:n.1533G>T
ENST00000527168.5:n.553G>T
ENST00000529957.5:n.616G>T
NM_032520.4:c.517G>T	NP_115909.1:p.Ala173Ser
XM_017023782.1:c.565G>T	XP_016879271.1:p.Ala189Ser
XM_017023783.1:c.157G>T	XP_016879272.1:p.Ala53Ser
NM_032520.5:c.517G>T MANE Select	NP_115909.1:p.Ala173Ser