Canonical Allele Identifier: CA394188534

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412688A>C (hg19) ; chr16:g.1362687A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362687A>C , CM000678.2:g.1362687A>C	GRCh38
NC_000016.9:g.1412688A>C , CM000678.1:g.1412688A>C	GRCh37
NC_000016.8:g.1352689A>C	NCBI36
NG_016985.1:g.15789A>C
NG_033129.1:g.57018T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.785A>C
ENST00000529110.2:c.770A>C	ENSP00000435349.2:p.Gln257Pro
ENST00000529957.6:n.744A>C
ENST00000683366.1:c.*418A>C	ENSP00000507283.1:n.*418A>C
ENST00000683887.1:c.734A>C	ENSP00000506886.1:p.Gln245Pro
ENST00000684100.1:n.680A>C
ENST00000684126.1:n.820A>C
ENST00000684688.1:n.1311A>C
ENST00000204679.9:c.686A>C MANE Select	ENSP00000204679.4:p.Gln229Pro
ENST00000204679.8:c.686A>C	ENSP00000204679.4:p.Gln229Pro
ENST00000527076.1:n.1909A>C
ENST00000527168.5:n.853A>C
ENST00000529957.5:n.785A>C
NM_032520.4:c.686A>C	NP_115909.1:p.Gln229Pro
XM_017023782.1:c.734A>C	XP_016879271.1:p.Gln245Pro
XM_017023783.1:c.326A>C	XP_016879272.1:p.Gln109Pro
NM_032520.5:c.686A>C MANE Select	NP_115909.1:p.Gln229Pro