Canonical Allele Identifier: CA394187907

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412291C>A (hg19) ; chr16:g.1362290C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362290C>A , CM000678.2:g.1362290C>A	GRCh38
NC_000016.9:g.1412291C>A , CM000678.1:g.1412291C>A	GRCh37
NC_000016.8:g.1352292C>A	NCBI36
NG_016985.1:g.15392C>A
NG_033129.1:g.57415G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.595C>A
ENST00000529110.2:c.580C>A	ENSP00000435349.2:p.Pro194Thr
ENST00000529957.6:n.554C>A
ENST00000683366.1:c.*228C>A	ENSP00000507283.1:n.*228C>A
ENST00000683887.1:c.544C>A	ENSP00000506886.1:p.Pro182Thr
ENST00000684100.1:n.490C>A
ENST00000684126.1:n.554C>A
ENST00000684688.1:n.1121C>A
ENST00000204679.9:c.496C>A MANE Select	ENSP00000204679.4:p.Pro166Thr
ENST00000204679.8:c.496C>A	ENSP00000204679.4:p.Pro166Thr
ENST00000527076.1:n.1512C>A
ENST00000527168.5:n.532C>A
ENST00000529957.5:n.595C>A
NM_032520.4:c.496C>A	NP_115909.1:p.Pro166Thr
XM_017023782.1:c.544C>A	XP_016879271.1:p.Pro182Thr
XM_017023783.1:c.136C>A	XP_016879272.1:p.Pro46Thr
NM_032520.5:c.496C>A MANE Select	NP_115909.1:p.Pro166Thr