Canonical Allele Identifier: CA394187240

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412066C>G (hg19) ; chr16:g.1362065C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362065C>G , CM000678.2:g.1362065C>G	GRCh38
NC_000016.9:g.1412066C>G , CM000678.1:g.1412066C>G	GRCh37
NC_000016.8:g.1352067C>G	NCBI36
NG_016985.1:g.15167C>G
NG_033129.1:g.57640G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.444C>G
ENST00000529110.2:c.429C>G	ENSP00000435349.2:p.Asn143Lys
ENST00000529957.6:n.403C>G
ENST00000683366.1:c.*77C>G	ENSP00000507283.1:n.*77C>G
ENST00000683887.1:c.393C>G	ENSP00000506886.1:p.Asn131Lys
ENST00000684100.1:n.339C>G
ENST00000684126.1:n.403C>G
ENST00000684688.1:n.970C>G
ENST00000204679.9:c.345C>G MANE Select	ENSP00000204679.4:p.Asn115Lys
ENST00000204679.8:c.345C>G	ENSP00000204679.4:p.Asn115Lys
ENST00000526820.5:c.*247C>G	ENSP00000434413.1:n.*247C>G
ENST00000527076.1:n.1361C>G
ENST00000527168.5:n.381C>G
ENST00000529110.1:c.412C>G
ENST00000529957.5:n.444C>G
NM_032520.4:c.345C>G	NP_115909.1:p.Asn115Lys
XM_017023782.1:c.393C>G	XP_016879271.1:p.Asn131Lys
XM_017023783.1:c.-16C>G	XP_016879272.1:n.-16C>G
NM_032520.5:c.345C>G MANE Select	NP_115909.1:p.Asn115Lys