Canonical Allele Identifier: CA394188789

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412889C>G (hg19) ; chr16:g.1362888C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362888C>G , CM000678.2:g.1362888C>G	GRCh38
NC_000016.9:g.1412889C>G , CM000678.1:g.1412889C>G	GRCh37
NC_000016.8:g.1352890C>G	NCBI36
NG_016985.1:g.15990C>G
NG_033129.1:g.56817G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.904C>G
ENST00000529110.2:c.889C>G	ENSP00000435349.2:p.Pro297Ala
ENST00000529957.6:n.863C>G
ENST00000683366.1:c.*537C>G	ENSP00000507283.1:n.*537C>G
ENST00000683887.1:c.853C>G	ENSP00000506886.1:p.Pro285Ala
ENST00000684100.1:n.799C>G
ENST00000684126.1:n.939C>G
ENST00000684688.1:n.1430C>G
ENST00000204679.9:c.805C>G MANE Select	ENSP00000204679.4:p.Pro269Ala
ENST00000204679.8:c.805C>G	ENSP00000204679.4:p.Pro269Ala
ENST00000527076.1:n.2028C>G
ENST00000527168.5:n.972C>G
ENST00000529957.5:n.904C>G
NM_032520.4:c.805C>G	NP_115909.1:p.Pro269Ala
XM_017023782.1:c.853C>G	XP_016879271.1:p.Pro285Ala
XM_017023783.1:c.445C>G	XP_016879272.1:p.Pro149Ala
NM_032520.5:c.805C>G MANE Select	NP_115909.1:p.Pro269Ala