Canonical Allele Identifier: CA2063741406

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489301_112489302delinsTC , CM000674.2:g.112489301_112489302delinsTC	GRCh38
NC_000012.11:g.112927105_112927106delinsTC , CM000674.1:g.112927105_112927106delinsTC	GRCh37
NC_000012.10:g.111411488_111411489delinsTC	NCBI36
NG_007459.1:g.75570_75571delinsTC , LRG_614:g.75570_75571delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1599+126_1599+127delinsTC	ENSP00000491593.2:n.1599+126_1599+127delinsTC
ENST00000685487.1:c.*114_*115delinsTC	ENSP00000508503.1:n.*114_*115delinsTC
ENST00000687624.1:n.390_391delinsTC
ENST00000687906.1:c.1485+126_1485+127delinsTC	ENSP00000509536.1:n.1485+126_1485+127delinsTC
ENST00000688597.1:c.1224+7096_1224+7097delinsTC	ENSP00000510628.1:n.1224+7096_1224+7097delinsTC
ENST00000688701.1:n.843+126_843+127delinsTC
ENST00000690210.1:c.1599+126_1599+127delinsTC	ENSP00000509272.1:n.1599+126_1599+127delinsTC
ENST00000690472.1:n.808+126_808+127delinsTC
ENST00000692624.1:c.*145+126_*145+127delinsTC	ENSP00000508953.1:n.*145+126_*145+127delinsTC
ENST00000351677.7:c.1599+126_1599+127delinsTC MANE Select	ENSP00000340944.3:n.1599+126_1599+127delinsTC
ENST00000351677.6:c.1599+126_1599+127delinsTC	ENSP00000340944.2:n.1599+126_1599+127delinsTC
ENST00000635625.1:c.1611+126_1611+127delinsTC	ENSP00000489597.1:n.1611+126_1611+127delinsTC
NM_002834.3:c.1599+126_1599+127delinsTC , LRG_614t1:c.1599+126_1599+127delinsTC	NP_002825.3:n.1599+126_1599+127delinsTC
XM_006719526.1:c.1611+126_1611+127delinsTC	XP_006719589.1:n.1611+126_1611+127delinsTC
XM_006719527.1:c.1497+126_1497+127delinsTC	XP_006719590.1:n.1497+126_1497+127delinsTC
XM_011538613.1:c.1608+126_1608+127delinsTC	XP_011536915.1:n.1608+126_1608+127delinsTC
NM_001330437.1:c.1611+126_1611+127delinsTC	NP_001317366.1:n.1611+126_1611+127delinsTC
NM_002834.4:c.1599+126_1599+127delinsTC	NP_002825.3:n.1599+126_1599+127delinsTC
XM_011538613.2:c.1608+126_1608+127delinsTC	XP_011536915.1:n.1608+126_1608+127delinsTC
XM_017019722.1:c.1596+126_1596+127delinsTC	XP_016875211.1:n.1596+126_1596+127delinsTC
NM_001330437.2:c.1611+126_1611+127delinsTC	NP_001317366.1:n.1611+126_1611+127delinsTC
NM_001374625.1:c.1596+126_1596+127delinsTC	NP_001361554.1:n.1596+126_1596+127delinsTC
NM_002834.5:c.1599+126_1599+127delinsTC MANE Select	NP_002825.3:n.1599+126_1599+127delinsTC