Canonical Allele Identifier: CA2621026819

Gene: PTPN11

Linked Data

• gnomAD v4: 12-112489316-C-CAAACTCCCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489316_112489317insAAACTCCCAA , CM000674.2:g.112489316_112489317insAAACTCCCAA	GRCh38
NC_000012.11:g.112927120_112927121insAAACTCCCAA , CM000674.1:g.112927120_112927121insAAACTCCCAA	GRCh37
NC_000012.10:g.111411503_111411504insAAACTCCCAA	NCBI36
NG_007459.1:g.75585_75586insAAACTCCCAA , LRG_614:g.75585_75586insAAACTCCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1599+141_1599+142insAAACTCCCAA	ENSP00000491593.2:n.1599+141_1599+142insAAACTCCCAA
ENST00000685487.1:c.*129_*130insAAACTCCCAA	ENSP00000508503.1:n.*129_*130insAAACTCCCAA
ENST00000687624.1:n.405_406insAAACTCCCAA
ENST00000687906.1:c.1485+141_1485+142insAAACTCCCAA	ENSP00000509536.1:n.1485+141_1485+142insAAACTCCCAA
ENST00000688597.1:c.1224+7111_1224+7112insAAACTCCCAA	ENSP00000510628.1:n.1224+7111_1224+7112insAAACTCCCAA
ENST00000688701.1:n.843+141_843+142insAAACTCCCAA
ENST00000690210.1:c.1599+141_1599+142insAAACTCCCAA	ENSP00000509272.1:n.1599+141_1599+142insAAACTCCCAA
ENST00000690472.1:n.808+141_808+142insAAACTCCCAA
ENST00000692624.1:c.*145+141_*145+142insAAACTCCCAA	ENSP00000508953.1:n.*145+141_*145+142insAAACTCCCAA
ENST00000351677.7:c.1599+141_1599+142insAAACTCCCAA MANE Select	ENSP00000340944.3:n.1599+141_1599+142insAAACTCCCAA
ENST00000351677.6:c.1599+141_1599+142insAAACTCCCAA	ENSP00000340944.2:n.1599+141_1599+142insAAACTCCCAA
ENST00000635625.1:c.1611+141_1611+142insAAACTCCCAA	ENSP00000489597.1:n.1611+141_1611+142insAAACTCCCAA
NM_002834.3:c.1599+141_1599+142insAAACTCCCAA , LRG_614t1:c.1599+141_1599+142insAAACTCCCAA	NP_002825.3:n.1599+141_1599+142insAAACTCCCAA
XM_006719526.1:c.1611+141_1611+142insAAACTCCCAA	XP_006719589.1:n.1611+141_1611+142insAAACTCCCAA
XM_006719527.1:c.1497+141_1497+142insAAACTCCCAA	XP_006719590.1:n.1497+141_1497+142insAAACTCCCAA
XM_011538613.1:c.1608+141_1608+142insAAACTCCCAA	XP_011536915.1:n.1608+141_1608+142insAAACTCCCAA
NM_001330437.1:c.1611+141_1611+142insAAACTCCCAA	NP_001317366.1:n.1611+141_1611+142insAAACTCCCAA
NM_002834.4:c.1599+141_1599+142insAAACTCCCAA	NP_002825.3:n.1599+141_1599+142insAAACTCCCAA
XM_011538613.2:c.1608+141_1608+142insAAACTCCCAA	XP_011536915.1:n.1608+141_1608+142insAAACTCCCAA
XM_017019722.1:c.1596+141_1596+142insAAACTCCCAA	XP_016875211.1:n.1596+141_1596+142insAAACTCCCAA
NM_001330437.2:c.1611+141_1611+142insAAACTCCCAA	NP_001317366.1:n.1611+141_1611+142insAAACTCCCAA
NM_001374625.1:c.1596+141_1596+142insAAACTCCCAA	NP_001361554.1:n.1596+141_1596+142insAAACTCCCAA
NM_002834.5:c.1599+141_1599+142insAAACTCCCAA MANE Select	NP_002825.3:n.1599+141_1599+142insAAACTCCCAA