Canonical Allele Identifier: CA394186802

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1411887T>G (hg19) ; chr16:g.1361886T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361886T>G , CM000678.2:g.1361886T>G	GRCh38
NC_000016.9:g.1411887T>G , CM000678.1:g.1411887T>G	GRCh37
NC_000016.8:g.1351888T>G	NCBI36
NG_016985.1:g.14988T>G
NG_033129.1:g.57819A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.347T>G
ENST00000529110.2:c.332T>G	ENSP00000435349.2:p.Phe111Cys
ENST00000529957.6:n.306T>G
ENST00000683366.1:c.193T>G	ENSP00000507283.1:p.Ser65Ala
ENST00000683887.1:c.296T>G	ENSP00000506886.1:p.Phe99Cys
ENST00000684100.1:n.242T>G
ENST00000684126.1:n.306T>G
ENST00000684688.1:n.873T>G
ENST00000204679.9:c.248T>G MANE Select	ENSP00000204679.4:p.Phe83Cys
ENST00000204679.8:c.248T>G	ENSP00000204679.4:p.Phe83Cys
ENST00000526820.5:c.*150T>G	ENSP00000434413.1:n.*150T>G
ENST00000527076.1:n.1264T>G
ENST00000527168.5:n.284T>G
ENST00000529110.1:c.315T>G
ENST00000529957.5:n.347T>G
NM_032520.4:c.248T>G	NP_115909.1:p.Phe83Cys
XM_017023782.1:c.296T>G	XP_016879271.1:p.Phe99Cys
XM_017023783.1:c.-113T>G	XP_016879272.1:n.-113T>G
NM_032520.5:c.248T>G MANE Select	NP_115909.1:p.Phe83Cys