Canonical Allele Identifier: CA394187241

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412067A>G (hg19) ; chr16:g.1362066A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362066A>G , CM000678.2:g.1362066A>G	GRCh38
NC_000016.9:g.1412067A>G , CM000678.1:g.1412067A>G	GRCh37
NC_000016.8:g.1352068A>G	NCBI36
NG_016985.1:g.15168A>G
NG_033129.1:g.57639T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.445A>G
ENST00000529110.2:c.430A>G	ENSP00000435349.2:p.Asn144Asp
ENST00000529957.6:n.404A>G
ENST00000683366.1:c.*78A>G	ENSP00000507283.1:n.*78A>G
ENST00000683887.1:c.394A>G	ENSP00000506886.1:p.Asn132Asp
ENST00000684100.1:n.340A>G
ENST00000684126.1:n.404A>G
ENST00000684688.1:n.971A>G
ENST00000204679.9:c.346A>G MANE Select	ENSP00000204679.4:p.Asn116Asp
ENST00000204679.8:c.346A>G	ENSP00000204679.4:p.Asn116Asp
ENST00000526820.5:c.*248A>G	ENSP00000434413.1:n.*248A>G
ENST00000527076.1:n.1362A>G
ENST00000527168.5:n.382A>G
ENST00000529110.1:c.413A>G
ENST00000529957.5:n.445A>G
NM_032520.4:c.346A>G	NP_115909.1:p.Asn116Asp
XM_017023782.1:c.394A>G	XP_016879271.1:p.Asn132Asp
XM_017023783.1:c.-15A>G	XP_016879272.1:n.-15A>G
NM_032520.5:c.346A>G MANE Select	NP_115909.1:p.Asn116Asp