Canonical Allele Identifier: CA2063740962

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489076G= , CM000674.2:g.112489076G=	GRCh38
NC_000012.11:g.112926880G= , CM000674.1:g.112926880G=	GRCh37
NC_000012.10:g.111411263G=	NCBI36
NG_007459.1:g.75345G= , LRG_614:g.75345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1500G=	ENSP00000491593.2:p.Gln500=
ENST00000685487.1:c.1500G=	ENSP00000508503.1:p.Gln500=
ENST00000687624.1:n.165G=
ENST00000687906.1:c.1386G=	ENSP00000509536.1:p.Gln462=
ENST00000688597.1:c.1224+6871G=	ENSP00000510628.1:n.1224+6871G=
ENST00000688701.1:n.744G=
ENST00000690210.1:c.1500G=	ENSP00000509272.1:p.Gln500=
ENST00000690472.1:n.709G=
ENST00000692624.1:c.*46G=	ENSP00000508953.1:n.*46G=
ENST00000351677.7:c.1500G= MANE Select	ENSP00000340944.3:p.Gln500=
ENST00000351677.6:c.1500G=	ENSP00000340944.2:p.Gln500=
ENST00000635625.1:c.1512G=	ENSP00000489597.1:p.Gln504=
ENST00000635652.1:c.513G=	ENSP00000489541.1:p.Gln171=
NM_002834.3:c.1500G= , LRG_614t1:c.1500G=	NP_002825.3:p.Gln500=
XM_006719526.1:c.1512G=	XP_006719589.1:p.Gln504=
XM_006719527.1:c.1398G=	XP_006719590.1:p.Gln466=
XM_011538613.1:c.1509G=	XP_011536915.1:p.Gln503=
NM_001330437.1:c.1512G=	NP_001317366.1:p.Gln504=
NM_002834.4:c.1500G=	NP_002825.3:p.Gln500=
XM_011538613.2:c.1509G=	XP_011536915.1:p.Gln503=
XM_017019722.1:c.1497G=	XP_016875211.1:p.Gln499=
NM_001330437.2:c.1512G=	NP_001317366.1:p.Gln504=
NM_001374625.1:c.1497G=	NP_001361554.1:p.Gln499=
NM_002834.5:c.1500G= MANE Select	NP_002825.3:p.Gln500=