Canonical Allele Identifier: CA394187206

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412051G>C (hg19) ; chr16:g.1362050G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362050G>C , CM000678.2:g.1362050G>C	GRCh38
NC_000016.9:g.1412051G>C , CM000678.1:g.1412051G>C	GRCh37
NC_000016.8:g.1352052G>C	NCBI36
NG_016985.1:g.15152G>C
NG_033129.1:g.57655C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.429G>C
ENST00000529110.2:c.414G>C	ENSP00000435349.2:p.Glu138Asp
ENST00000529957.6:n.388G>C
ENST00000683366.1:c.*62G>C	ENSP00000507283.1:n.*62G>C
ENST00000683887.1:c.378G>C	ENSP00000506886.1:p.Glu126Asp
ENST00000684100.1:n.324G>C
ENST00000684126.1:n.388G>C
ENST00000684688.1:n.955G>C
ENST00000204679.9:c.330G>C MANE Select	ENSP00000204679.4:p.Glu110Asp
ENST00000204679.8:c.330G>C	ENSP00000204679.4:p.Glu110Asp
ENST00000526820.5:c.*232G>C	ENSP00000434413.1:n.*232G>C
ENST00000527076.1:n.1346G>C
ENST00000527168.5:n.366G>C
ENST00000529110.1:c.397G>C
ENST00000529957.5:n.429G>C
NM_032520.4:c.330G>C	NP_115909.1:p.Glu110Asp
XM_017023782.1:c.378G>C	XP_016879271.1:p.Glu126Asp
XM_017023783.1:c.-31G>C	XP_016879272.1:n.-31G>C
NM_032520.5:c.330G>C MANE Select	NP_115909.1:p.Glu110Asp