Canonical Allele Identifier: CA394188423

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412633A>G (hg19) ; chr16:g.1362632A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362632A>G , CM000678.2:g.1362632A>G	GRCh38
NC_000016.9:g.1412633A>G , CM000678.1:g.1412633A>G	GRCh37
NC_000016.8:g.1352634A>G	NCBI36
NG_016985.1:g.15734A>G
NG_033129.1:g.57073T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.730A>G
ENST00000529110.2:c.715A>G	ENSP00000435349.2:p.Thr239Ala
ENST00000529957.6:n.689A>G
ENST00000683366.1:c.*363A>G	ENSP00000507283.1:n.*363A>G
ENST00000683887.1:c.679A>G	ENSP00000506886.1:p.Thr227Ala
ENST00000684100.1:n.625A>G
ENST00000684126.1:n.765A>G
ENST00000684688.1:n.1256A>G
ENST00000204679.9:c.631A>G MANE Select	ENSP00000204679.4:p.Thr211Ala
ENST00000204679.8:c.631A>G	ENSP00000204679.4:p.Thr211Ala
ENST00000527076.1:n.1854A>G
ENST00000527168.5:n.798A>G
ENST00000529957.5:n.730A>G
NM_032520.4:c.631A>G	NP_115909.1:p.Thr211Ala
XM_017023782.1:c.679A>G	XP_016879271.1:p.Thr227Ala
XM_017023783.1:c.271A>G	XP_016879272.1:p.Thr91Ala
NM_032520.5:c.631A>G MANE Select	NP_115909.1:p.Thr211Ala