Canonical Allele Identifier: CA2063740996

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489082_112489083delinsAG , CM000674.2:g.112489082_112489083delinsAG	GRCh38
NC_000012.11:g.112926886_112926887delinsAG , CM000674.1:g.112926886_112926887delinsAG	GRCh37
NC_000012.10:g.111411269_111411270delinsAG	NCBI36
NG_007459.1:g.75351_75352delinsAG , LRG_614:g.75351_75352delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1506_1507delinsAG	ENSP00000491593.2:p.Ser502=
ENST00000685487.1:c.1506_1507delinsAG	ENSP00000508503.1:p.Ser502=
ENST00000687624.1:n.171_172delinsAG
ENST00000687906.1:c.1392_1393delinsAG	ENSP00000509536.1:p.Ser464=
ENST00000688597.1:c.1224+6877_1224+6878delinsAG	ENSP00000510628.1:n.1224+6877_1224+6878delinsAG
ENST00000688701.1:n.750_751delinsAG
ENST00000690210.1:c.1506_1507delinsAG	ENSP00000509272.1:p.Ser502=
ENST00000690472.1:n.715_716delinsAG
ENST00000692624.1:c.*52_*53delinsAG	ENSP00000508953.1:n.*52_*53delinsAG
ENST00000351677.7:c.1506_1507delinsAG MANE Select	ENSP00000340944.3:p.Ser502=
ENST00000351677.6:c.1506_1507delinsAG	ENSP00000340944.2:p.Ser502=
ENST00000635625.1:c.1518_1519delinsAG	ENSP00000489597.1:p.Ser506=
ENST00000635652.1:c.519_520delinsAG	ENSP00000489541.1:p.Ser173=
NM_002834.3:c.1506_1507delinsAG , LRG_614t1:c.1506_1507delinsAG	NP_002825.3:p.Ser502=
XM_006719526.1:c.1518_1519delinsAG	XP_006719589.1:p.Ser506=
XM_006719527.1:c.1404_1405delinsAG	XP_006719590.1:p.Ser468=
XM_011538613.1:c.1515_1516delinsAG	XP_011536915.1:p.Ser505=
NM_001330437.1:c.1518_1519delinsAG	NP_001317366.1:p.Ser506=
NM_002834.4:c.1506_1507delinsAG	NP_002825.3:p.Ser502=
XM_011538613.2:c.1515_1516delinsAG	XP_011536915.1:p.Ser505=
XM_017019722.1:c.1503_1504delinsAG	XP_016875211.1:p.Ser501=
NM_001330437.2:c.1518_1519delinsAG	NP_001317366.1:p.Ser506=
NM_001374625.1:c.1503_1504delinsAG	NP_001361554.1:p.Ser501=
NM_002834.5:c.1506_1507delinsAG MANE Select	NP_002825.3:p.Ser502=