Canonical Allele Identifier: CA2830551883

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489194_112489195insTAC , CM000674.2:g.112489194_112489195insTAC	GRCh38
NC_000012.11:g.112926998_112926999insTAC , CM000674.1:g.112926998_112926999insTAC	GRCh37
NC_000012.10:g.111411381_111411382insTAC	NCBI36
NG_007459.1:g.75463_75464insTAC , LRG_614:g.75463_75464insTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1599+19_1599+20insTAC	ENSP00000491593.2:n.1599+19_1599+20insTAC
ENST00000685487.1:c.*7_*8insTAC	ENSP00000508503.1:n.*7_*8insTAC
ENST00000687624.1:n.283_284insTAC
ENST00000687906.1:c.1485+19_1485+20insTAC	ENSP00000509536.1:n.1485+19_1485+20insTAC
ENST00000688597.1:c.1224+6989_1224+6990insTAC	ENSP00000510628.1:n.1224+6989_1224+6990insTAC
ENST00000688701.1:n.843+19_843+20insTAC
ENST00000690210.1:c.1599+19_1599+20insTAC	ENSP00000509272.1:n.1599+19_1599+20insTAC
ENST00000690472.1:n.808+19_808+20insTAC
ENST00000692624.1:c.*145+19_*145+20insTAC	ENSP00000508953.1:n.*145+19_*145+20insTAC
ENST00000351677.7:c.1599+19_1599+20insTAC MANE Select	ENSP00000340944.3:n.1599+19_1599+20insTAC
ENST00000351677.6:c.1599+19_1599+20insTAC	ENSP00000340944.2:n.1599+19_1599+20insTAC
ENST00000635625.1:c.1611+19_1611+20insTAC	ENSP00000489597.1:n.1611+19_1611+20insTAC
NM_002834.3:c.1599+19_1599+20insTAC , LRG_614t1:c.1599+19_1599+20insTAC	NP_002825.3:n.1599+19_1599+20insTAC
XM_006719526.1:c.1611+19_1611+20insTAC	XP_006719589.1:n.1611+19_1611+20insTAC
XM_006719527.1:c.1497+19_1497+20insTAC	XP_006719590.1:n.1497+19_1497+20insTAC
XM_011538613.1:c.1608+19_1608+20insTAC	XP_011536915.1:n.1608+19_1608+20insTAC
NM_001330437.1:c.1611+19_1611+20insTAC	NP_001317366.1:n.1611+19_1611+20insTAC
NM_002834.4:c.1599+19_1599+20insTAC	NP_002825.3:n.1599+19_1599+20insTAC
XM_011538613.2:c.1608+19_1608+20insTAC	XP_011536915.1:n.1608+19_1608+20insTAC
XM_017019722.1:c.1596+19_1596+20insTAC	XP_016875211.1:n.1596+19_1596+20insTAC
NM_001330437.2:c.1611+19_1611+20insTAC	NP_001317366.1:n.1611+19_1611+20insTAC
NM_001374625.1:c.1596+19_1596+20insTAC	NP_001361554.1:n.1596+19_1596+20insTAC
NM_002834.5:c.1599+19_1599+20insTAC MANE Select	NP_002825.3:n.1599+19_1599+20insTAC