Canonical Allele Identifier: CA394188345

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412524A>T (hg19) ; chr16:g.1362523A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362523A>T , CM000678.2:g.1362523A>T	GRCh38
NC_000016.9:g.1412524A>T , CM000678.1:g.1412524A>T	GRCh37
NC_000016.8:g.1352525A>T	NCBI36
NG_016985.1:g.15625A>T
NG_033129.1:g.57182T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.697A>T
ENST00000529110.2:c.682A>T	ENSP00000435349.2:p.Ile228Phe
ENST00000529957.6:n.656A>T
ENST00000683366.1:c.*330A>T	ENSP00000507283.1:n.*330A>T
ENST00000683887.1:c.646A>T	ENSP00000506886.1:p.Ile216Phe
ENST00000684100.1:n.592A>T
ENST00000684126.1:n.656A>T
ENST00000684688.1:n.1223A>T
ENST00000204679.9:c.598A>T MANE Select	ENSP00000204679.4:p.Ile200Phe
ENST00000204679.8:c.598A>T	ENSP00000204679.4:p.Ile200Phe
ENST00000527076.1:n.1745A>T
ENST00000527168.5:n.765A>T
ENST00000529957.5:n.697A>T
NM_032520.4:c.598A>T	NP_115909.1:p.Ile200Phe
XM_017023782.1:c.646A>T	XP_016879271.1:p.Ile216Phe
XM_017023783.1:c.238A>T	XP_016879272.1:p.Ile80Phe
NM_032520.5:c.598A>T MANE Select	NP_115909.1:p.Ile200Phe