Canonical Allele Identifier: CA493026488

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412221T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362220T>C , CM000678.2:g.1362220T>C	GRCh38
NC_000016.9:g.1412221T>C , CM000678.1:g.1412221T>C	GRCh37
NC_000016.8:g.1352222T>C	NCBI36
NG_016985.1:g.15322T>C
NG_033129.1:g.57485A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.525T>C
ENST00000529110.2:c.510T>C	ENSP00000435349.2:p.Cys170=
ENST00000529957.6:n.484T>C
ENST00000683366.1:c.*158T>C	ENSP00000507283.1:n.*158T>C
ENST00000683887.1:c.474T>C	ENSP00000506886.1:p.Cys158=
ENST00000684100.1:n.420T>C
ENST00000684126.1:n.484T>C
ENST00000684688.1:n.1051T>C
ENST00000204679.9:c.426T>C MANE Select	ENSP00000204679.4:p.Cys142=
ENST00000204679.8:c.426T>C	ENSP00000204679.4:p.Cys142=
ENST00000527076.1:n.1442T>C
ENST00000527168.5:n.462T>C
ENST00000529110.1:c.493T>C
ENST00000529957.5:n.525T>C
NM_032520.4:c.426T>C	NP_115909.1:p.Cys142=
XM_017023782.1:c.474T>C	XP_016879271.1:p.Cys158=
XM_017023783.1:c.66T>C	XP_016879272.1:p.Cys22=
NM_032520.5:c.426T>C MANE Select	NP_115909.1:p.Cys142=