Canonical Allele Identifier: CA493026569

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412314C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362313C>T , CM000678.2:g.1362313C>T	GRCh38
NC_000016.9:g.1412314C>T , CM000678.1:g.1412314C>T	GRCh37
NC_000016.8:g.1352315C>T	NCBI36
NG_016985.1:g.15415C>T
NG_033129.1:g.57392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.618C>T
ENST00000529110.2:c.603C>T	ENSP00000435349.2:p.Ala201=
ENST00000529957.6:n.577C>T
ENST00000683366.1:c.*251C>T	ENSP00000507283.1:n.*251C>T
ENST00000683887.1:c.567C>T	ENSP00000506886.1:p.Ala189=
ENST00000684100.1:n.513C>T
ENST00000684126.1:n.577C>T
ENST00000684688.1:n.1144C>T
ENST00000204679.9:c.519C>T MANE Select	ENSP00000204679.4:p.Ala173=
ENST00000204679.8:c.519C>T	ENSP00000204679.4:p.Ala173=
ENST00000527076.1:n.1535C>T
ENST00000527168.5:n.555C>T
ENST00000529957.5:n.618C>T
NM_032520.4:c.519C>T	NP_115909.1:p.Ala173=
XM_017023782.1:c.567C>T	XP_016879271.1:p.Ala189=
XM_017023783.1:c.159C>T	XP_016879272.1:p.Ala53=
NM_032520.5:c.519C>T MANE Select	NP_115909.1:p.Ala173=