Canonical Allele Identifier: CA394188783

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412886A>T (hg19) ; chr16:g.1362885A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362885A>T , CM000678.2:g.1362885A>T	GRCh38
NC_000016.9:g.1412886A>T , CM000678.1:g.1412886A>T	GRCh37
NC_000016.8:g.1352887A>T	NCBI36
NG_016985.1:g.15987A>T
NG_033129.1:g.56820T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.901A>T
ENST00000529110.2:c.886A>T	ENSP00000435349.2:p.Ile296Phe
ENST00000529957.6:n.860A>T
ENST00000683366.1:c.*534A>T	ENSP00000507283.1:n.*534A>T
ENST00000683887.1:c.850A>T	ENSP00000506886.1:p.Ile284Phe
ENST00000684100.1:n.796A>T
ENST00000684126.1:n.936A>T
ENST00000684688.1:n.1427A>T
ENST00000204679.9:c.802A>T MANE Select	ENSP00000204679.4:p.Ile268Phe
ENST00000204679.8:c.802A>T	ENSP00000204679.4:p.Ile268Phe
ENST00000527076.1:n.2025A>T
ENST00000527168.5:n.969A>T
ENST00000529957.5:n.901A>T
NM_032520.4:c.802A>T	NP_115909.1:p.Ile268Phe
XM_017023782.1:c.850A>T	XP_016879271.1:p.Ile284Phe
XM_017023783.1:c.442A>T	XP_016879272.1:p.Ile148Phe
NM_032520.5:c.802A>T MANE Select	NP_115909.1:p.Ile268Phe