Canonical Allele Identifier: CA394188820

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412904A>G (hg19) ; chr16:g.1362903A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362903A>G , CM000678.2:g.1362903A>G	GRCh38
NC_000016.9:g.1412904A>G , CM000678.1:g.1412904A>G	GRCh37
NC_000016.8:g.1352905A>G	NCBI36
NG_016985.1:g.16005A>G
NG_033129.1:g.56802T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.919A>G
ENST00000529110.2:c.904A>G	ENSP00000435349.2:p.Thr302Ala
ENST00000529957.6:n.878A>G
ENST00000683366.1:c.*552A>G	ENSP00000507283.1:n.*552A>G
ENST00000683887.1:c.868A>G	ENSP00000506886.1:p.Thr290Ala
ENST00000684100.1:n.814A>G
ENST00000684126.1:n.954A>G
ENST00000684688.1:n.1445A>G
ENST00000204679.9:c.820A>G MANE Select	ENSP00000204679.4:p.Thr274Ala
ENST00000204679.8:c.820A>G	ENSP00000204679.4:p.Thr274Ala
ENST00000527076.1:n.2043A>G
ENST00000527168.5:n.987A>G
ENST00000529957.5:n.919A>G
NM_032520.4:c.820A>G	NP_115909.1:p.Thr274Ala
XM_017023782.1:c.868A>G	XP_016879271.1:p.Thr290Ala
XM_017023783.1:c.460A>G	XP_016879272.1:p.Thr154Ala
NM_032520.5:c.820A>G MANE Select	NP_115909.1:p.Thr274Ala