Canonical Allele Identifier: CA2063740116

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112488444G= , CM000674.2:g.112488444G=	GRCh38
NC_000012.11:g.112926248G= , CM000674.1:g.112926248G=	GRCh37
NC_000012.10:g.111410631G=	NCBI36
NG_007459.1:g.74713G= , LRG_614:g.74713G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1381G=	ENSP00000491593.2:p.Ala461=
ENST00000685487.1:c.1381G=	ENSP00000508503.1:p.Ala461=
ENST00000687624.1:n.46G=
ENST00000687906.1:c.1267G=	ENSP00000509536.1:p.Ala423=
ENST00000688597.1:c.1224+6239G=	ENSP00000510628.1:n.1224+6239G=
ENST00000688701.1:n.625G=
ENST00000690210.1:c.1381G=	ENSP00000509272.1:p.Ala461=
ENST00000690472.1:n.590G=
ENST00000692624.1:c.1380-580G=	ENSP00000508953.1:n.1380-580G=
ENST00000351677.7:c.1381G= MANE Select	ENSP00000340944.3:p.Ala461=
ENST00000351677.6:c.1381G=	ENSP00000340944.2:p.Ala461=
ENST00000635625.1:c.1393G=	ENSP00000489597.1:p.Ala465=
ENST00000635652.1:c.394G=	ENSP00000489541.1:p.Ala132=
NM_002834.3:c.1381G= , LRG_614t1:c.1381G=	NP_002825.3:p.Ala461=
XM_006719526.1:c.1393G=	XP_006719589.1:p.Ala465=
XM_006719527.1:c.1279G=	XP_006719590.1:p.Ala427=
XM_011538613.1:c.1390G=	XP_011536915.1:p.Ala464=
NM_001330437.1:c.1393G=	NP_001317366.1:p.Ala465=
NM_002834.4:c.1381G=	NP_002825.3:p.Ala461=
XM_011538613.2:c.1390G=	XP_011536915.1:p.Ala464=
XM_017019722.1:c.1378G=	XP_016875211.1:p.Ala460=
NM_001330437.2:c.1393G=	NP_001317366.1:p.Ala465=
NM_001374625.1:c.1378G=	NP_001361554.1:p.Ala460=
NM_002834.5:c.1381G= MANE Select	NP_002825.3:p.Ala461=