Canonical Allele Identifier: CA2063755316

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112502151A= , CM000674.2:g.112502151A=	GRCh38
NC_000012.11:g.112939955A= , CM000674.1:g.112939955A=	GRCh37
NC_000012.10:g.111424338A=	NCBI36
NG_007459.1:g.88420A= , LRG_614:g.88420A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1607A=	ENSP00000491593.2:p.Lys536=
ENST00000685487.1:c.*809A=	ENSP00000508503.1:n.*809A=
ENST00000687120.1:n.990A=
ENST00000687906.1:c.1493A=	ENSP00000509536.1:p.Lys498=
ENST00000688597.1:c.1232A=	ENSP00000510628.1:p.Lys411=
ENST00000688701.1:n.851A=
ENST00000690210.1:c.1607A=	ENSP00000509272.1:p.Lys536=
ENST00000690472.1:n.816A=
ENST00000692624.1:c.*153A=	ENSP00000508953.1:n.*153A=
ENST00000351677.7:c.1607A= MANE Select	ENSP00000340944.3:p.Lys536=
ENST00000351677.6:c.1607A=	ENSP00000340944.2:p.Lys536=
ENST00000635625.1:c.1619A=	ENSP00000489597.1:p.Lys540=
NM_002834.3:c.1607A= , LRG_614t1:c.1607A=	NP_002825.3:p.Lys536=
XM_006719526.1:c.1619A=	XP_006719589.1:p.Lys540=
XM_006719527.1:c.1505A=	XP_006719590.1:p.Lys502=
XM_011538613.1:c.1616A=	XP_011536915.1:p.Lys539=
NM_001330437.1:c.1619A=	NP_001317366.1:p.Lys540=
NM_002834.4:c.1607A=	NP_002825.3:p.Lys536=
XM_011538613.2:c.1616A=	XP_011536915.1:p.Lys539=
XM_017019722.1:c.1604A=	XP_016875211.1:p.Lys535=
NM_001330437.2:c.1619A=	NP_001317366.1:p.Lys540=
NM_001374625.1:c.1604A=	NP_001361554.1:p.Lys535=
NM_002834.5:c.1607A= MANE Select	NP_002825.3:p.Lys536=