Canonical Allele Identifier: CA394186864

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1411902A>T (hg19) ; chr16:g.1361901A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361901A>T , CM000678.2:g.1361901A>T	GRCh38
NC_000016.9:g.1411902A>T , CM000678.1:g.1411902A>T	GRCh37
NC_000016.8:g.1351903A>T	NCBI36
NG_016985.1:g.15003A>T
NG_033129.1:g.57804T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.362A>T
ENST00000529110.2:c.347A>T	ENSP00000435349.2:p.Asn116Ile
ENST00000529957.6:n.321A>T
ENST00000683366.1:c.208A>T	ENSP00000507283.1:p.Thr70Ser
ENST00000683887.1:c.311A>T	ENSP00000506886.1:p.Asn104Ile
ENST00000684100.1:n.257A>T
ENST00000684126.1:n.321A>T
ENST00000684688.1:n.888A>T
ENST00000204679.9:c.263A>T MANE Select	ENSP00000204679.4:p.Asn88Ile
ENST00000204679.8:c.263A>T	ENSP00000204679.4:p.Asn88Ile
ENST00000526820.5:c.*165A>T	ENSP00000434413.1:n.*165A>T
ENST00000527076.1:n.1279A>T
ENST00000527168.5:n.299A>T
ENST00000529110.1:c.330A>T
ENST00000529957.5:n.362A>T
NM_032520.4:c.263A>T	NP_115909.1:p.Asn88Ile
XM_017023782.1:c.311A>T	XP_016879271.1:p.Asn104Ile
XM_017023783.1:c.-98A>T	XP_016879272.1:n.-98A>T
NM_032520.5:c.263A>T MANE Select	NP_115909.1:p.Asn88Ile