Canonical Allele Identifier: CA394188348

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412525T>G (hg19) ; chr16:g.1362524T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362524T>G , CM000678.2:g.1362524T>G	GRCh38
NC_000016.9:g.1412525T>G , CM000678.1:g.1412525T>G	GRCh37
NC_000016.8:g.1352526T>G	NCBI36
NG_016985.1:g.15626T>G
NG_033129.1:g.57181A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.698T>G
ENST00000529110.2:c.683T>G	ENSP00000435349.2:p.Ile228Ser
ENST00000529957.6:n.657T>G
ENST00000683366.1:c.*331T>G	ENSP00000507283.1:n.*331T>G
ENST00000683887.1:c.647T>G	ENSP00000506886.1:p.Ile216Ser
ENST00000684100.1:n.593T>G
ENST00000684126.1:n.657T>G
ENST00000684688.1:n.1224T>G
ENST00000204679.9:c.599T>G MANE Select	ENSP00000204679.4:p.Ile200Ser
ENST00000204679.8:c.599T>G	ENSP00000204679.4:p.Ile200Ser
ENST00000527076.1:n.1746T>G
ENST00000527168.5:n.766T>G
ENST00000529957.5:n.698T>G
NM_032520.4:c.599T>G	NP_115909.1:p.Ile200Ser
XM_017023782.1:c.647T>G	XP_016879271.1:p.Ile216Ser
XM_017023783.1:c.239T>G	XP_016879272.1:p.Ile80Ser
NM_032520.5:c.599T>G MANE Select	NP_115909.1:p.Ile200Ser