Canonical Allele Identifier: CA2063743487

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112453319_112453325delinsACTGGTG , CM000674.2:g.112453319_112453325delinsACTGGTG	GRCh38
NC_000012.11:g.112891123_112891129delinsACTGGTG , CM000674.1:g.112891123_112891129delinsACTGGTG	GRCh37
NC_000012.10:g.111375506_111375512delinsACTGGTG	NCBI36
NG_007459.1:g.39588_39594delinsACTGGTG , LRG_614:g.39588_39594delinsACTGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.457_463delinsACTGGTG	ENSP00000491593.2:p.Thr153=
ENST00000685487.1:c.457_463delinsACTGGTG	ENSP00000508503.1:p.Thr153=
ENST00000687906.1:c.457_463delinsACTGGTG	ENSP00000509536.1:p.Thr153=
ENST00000688597.1:c.457_463delinsACTGGTG	ENSP00000510628.1:p.Thr153=
ENST00000690210.1:c.457_463delinsACTGGTG	ENSP00000509272.1:p.Thr153=
ENST00000692624.1:c.457_463delinsACTGGTG	ENSP00000508953.1:p.Thr153=
ENST00000351677.7:c.457_463delinsACTGGTG MANE Select	ENSP00000340944.3:p.Thr153=
ENST00000639857.1:c.457_463delinsACTGGTG	ENSP00000491593.1:p.Thr153=
ENST00000351677.6:c.457_463delinsACTGGTG	ENSP00000340944.2:p.Thr153=
ENST00000392597.5:c.457_463delinsACTGGTG	ENSP00000376376.1:p.Thr153=
ENST00000635625.1:c.457_463delinsACTGGTG	ENSP00000489597.1:p.Thr153=
NM_002834.3:c.457_463delinsACTGGTG , LRG_614t1:c.457_463delinsACTGGTG	NP_002825.3:p.Thr153=
NM_080601.1:c.457_463delinsACTGGTG	NP_542168.1:p.Thr153=
XM_006719526.1:c.457_463delinsACTGGTG	XP_006719589.1:p.Thr153=
XM_006719527.1:c.457_463delinsACTGGTG	XP_006719590.1:p.Thr153=
XM_011538613.1:c.454_460delinsACTGGTG	XP_011536915.1:p.Thr152=
NM_001330437.1:c.457_463delinsACTGGTG	NP_001317366.1:p.Thr153=
NM_002834.4:c.457_463delinsACTGGTG	NP_002825.3:p.Thr153=
NM_080601.2:c.457_463delinsACTGGTG	NP_542168.1:p.Thr153=
XM_011538613.2:c.454_460delinsACTGGTG	XP_011536915.1:p.Thr152=
XM_017019722.1:c.454_460delinsACTGGTG	XP_016875211.1:p.Thr152=
NM_001330437.2:c.457_463delinsACTGGTG	NP_001317366.1:p.Thr153=
NM_001374625.1:c.454_460delinsACTGGTG	NP_001361554.1:p.Thr152=
NM_002834.5:c.457_463delinsACTGGTG MANE Select	NP_002825.3:p.Thr153=
NM_080601.3:c.457_463delinsACTGGTG	NP_542168.1:p.Thr153=