Canonical Allele Identifier: CA493026601

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412466G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362465G>T , CM000678.2:g.1362465G>T	GRCh38
NC_000016.9:g.1412466G>T , CM000678.1:g.1412466G>T	GRCh37
NC_000016.8:g.1352467G>T	NCBI36
NG_016985.1:g.15567G>T
NG_033129.1:g.57240C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.639G>T
ENST00000529110.2:c.624G>T	ENSP00000435349.2:p.Leu208=
ENST00000529957.6:n.598G>T
ENST00000683366.1:c.*272G>T	ENSP00000507283.1:n.*272G>T
ENST00000683887.1:c.588G>T	ENSP00000506886.1:p.Leu196=
ENST00000684100.1:n.534G>T
ENST00000684126.1:n.598G>T
ENST00000684688.1:n.1165G>T
ENST00000204679.9:c.540G>T MANE Select	ENSP00000204679.4:p.Leu180=
ENST00000204679.8:c.540G>T	ENSP00000204679.4:p.Leu180=
ENST00000527076.1:n.1687G>T
ENST00000527168.5:n.707G>T
ENST00000529957.5:n.639G>T
NM_032520.4:c.540G>T	NP_115909.1:p.Leu180=
XM_017023782.1:c.588G>T	XP_016879271.1:p.Leu196=
XM_017023783.1:c.180G>T	XP_016879272.1:p.Leu60=
NM_032520.5:c.540G>T MANE Select	NP_115909.1:p.Leu180=