Canonical Allele Identifier: CA394188767

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412878A>C (hg19) ; chr16:g.1362877A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362877A>C , CM000678.2:g.1362877A>C	GRCh38
NC_000016.9:g.1412878A>C , CM000678.1:g.1412878A>C	GRCh37
NC_000016.8:g.1352879A>C	NCBI36
NG_016985.1:g.15979A>C
NG_033129.1:g.56828T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.893A>C
ENST00000529110.2:c.878A>C	ENSP00000435349.2:p.Gln293Pro
ENST00000529957.6:n.852A>C
ENST00000683366.1:c.*526A>C	ENSP00000507283.1:n.*526A>C
ENST00000683887.1:c.842A>C	ENSP00000506886.1:p.Gln281Pro
ENST00000684100.1:n.788A>C
ENST00000684126.1:n.928A>C
ENST00000684688.1:n.1419A>C
ENST00000204679.9:c.794A>C MANE Select	ENSP00000204679.4:p.Gln265Pro
ENST00000204679.8:c.794A>C	ENSP00000204679.4:p.Gln265Pro
ENST00000527076.1:n.2017A>C
ENST00000527168.5:n.961A>C
ENST00000529957.5:n.893A>C
NM_032520.4:c.794A>C	NP_115909.1:p.Gln265Pro
XM_017023782.1:c.842A>C	XP_016879271.1:p.Gln281Pro
XM_017023783.1:c.434A>C	XP_016879272.1:p.Gln145Pro
NM_032520.5:c.794A>C MANE Select	NP_115909.1:p.Gln265Pro