Canonical Allele Identifier: CA394187228

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412059T>G (hg19) ; chr16:g.1362058T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362058T>G , CM000678.2:g.1362058T>G	GRCh38
NC_000016.9:g.1412059T>G , CM000678.1:g.1412059T>G	GRCh37
NC_000016.8:g.1352060T>G	NCBI36
NG_016985.1:g.15160T>G
NG_033129.1:g.57647A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.437T>G
ENST00000529110.2:c.422T>G	ENSP00000435349.2:p.Ile141Ser
ENST00000529957.6:n.396T>G
ENST00000683366.1:c.*70T>G	ENSP00000507283.1:n.*70T>G
ENST00000683887.1:c.386T>G	ENSP00000506886.1:p.Ile129Ser
ENST00000684100.1:n.332T>G
ENST00000684126.1:n.396T>G
ENST00000684688.1:n.963T>G
ENST00000204679.9:c.338T>G MANE Select	ENSP00000204679.4:p.Ile113Ser
ENST00000204679.8:c.338T>G	ENSP00000204679.4:p.Ile113Ser
ENST00000526820.5:c.*240T>G	ENSP00000434413.1:n.*240T>G
ENST00000527076.1:n.1354T>G
ENST00000527168.5:n.374T>G
ENST00000529110.1:c.405T>G
ENST00000529957.5:n.437T>G
NM_032520.4:c.338T>G	NP_115909.1:p.Ile113Ser
XM_017023782.1:c.386T>G	XP_016879271.1:p.Ile129Ser
XM_017023783.1:c.-23T>G	XP_016879272.1:n.-23T>G
NM_032520.5:c.338T>G MANE Select	NP_115909.1:p.Ile113Ser