Canonical Allele Identifier: CA394187925

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412302C>G (hg19) ; chr16:g.1362301C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362301C>G , CM000678.2:g.1362301C>G	GRCh38
NC_000016.9:g.1412302C>G , CM000678.1:g.1412302C>G	GRCh37
NC_000016.8:g.1352303C>G	NCBI36
NG_016985.1:g.15403C>G
NG_033129.1:g.57404G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.606C>G
ENST00000529110.2:c.591C>G	ENSP00000435349.2:p.Cys197Trp
ENST00000529957.6:n.565C>G
ENST00000683366.1:c.*239C>G	ENSP00000507283.1:n.*239C>G
ENST00000683887.1:c.555C>G	ENSP00000506886.1:p.Cys185Trp
ENST00000684100.1:n.501C>G
ENST00000684126.1:n.565C>G
ENST00000684688.1:n.1132C>G
ENST00000204679.9:c.507C>G MANE Select	ENSP00000204679.4:p.Cys169Trp
ENST00000204679.8:c.507C>G	ENSP00000204679.4:p.Cys169Trp
ENST00000527076.1:n.1523C>G
ENST00000527168.5:n.543C>G
ENST00000529957.5:n.606C>G
NM_032520.4:c.507C>G	NP_115909.1:p.Cys169Trp
XM_017023782.1:c.555C>G	XP_016879271.1:p.Cys185Trp
XM_017023783.1:c.147C>G	XP_016879272.1:p.Cys49Trp
NM_032520.5:c.507C>G MANE Select	NP_115909.1:p.Cys169Trp