Canonical Allele Identifier: CA2063739473

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112449941_112449942delinsTG , CM000674.2:g.112449941_112449942delinsTG	GRCh38
NC_000012.11:g.112887745_112887746delinsTG , CM000674.1:g.112887745_112887746delinsTG	GRCh37
NC_000012.10:g.111372128_111372129delinsTG	NCBI36
NG_007459.1:g.36210_36211delinsTG , LRG_614:g.36210_36211delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.138-377_138-376delinsTG	ENSP00000491593.2:n.138-377_138-376delinsTG
ENST00000685487.1:c.138-377_138-376delinsTG	ENSP00000508503.1:n.138-377_138-376delinsTG
ENST00000687906.1:c.138-377_138-376delinsTG	ENSP00000509536.1:n.138-377_138-376delinsTG
ENST00000688597.1:c.138-377_138-376delinsTG	ENSP00000510628.1:n.138-377_138-376delinsTG
ENST00000690210.1:c.138-377_138-376delinsTG	ENSP00000509272.1:n.138-377_138-376delinsTG
ENST00000692624.1:c.138-377_138-376delinsTG	ENSP00000508953.1:n.138-377_138-376delinsTG
ENST00000351677.7:c.138-377_138-376delinsTG MANE Select	ENSP00000340944.3:n.138-377_138-376delinsTG
ENST00000639857.1:c.138-377_138-376delinsTG	ENSP00000491593.1:n.138-377_138-376delinsTG
ENST00000351677.6:c.138-377_138-376delinsTG	ENSP00000340944.2:n.138-377_138-376delinsTG
ENST00000392597.5:c.138-377_138-376delinsTG	ENSP00000376376.1:n.138-377_138-376delinsTG
ENST00000635625.1:c.138-377_138-376delinsTG	ENSP00000489597.1:n.138-377_138-376delinsTG
NM_002834.3:c.138-377_138-376delinsTG , LRG_614t1:c.138-377_138-376delinsTG	NP_002825.3:n.138-377_138-376delinsTG
NM_080601.1:c.138-377_138-376delinsTG	NP_542168.1:n.138-377_138-376delinsTG
XM_006719526.1:c.138-377_138-376delinsTG	XP_006719589.1:n.138-377_138-376delinsTG
XM_006719527.1:c.138-377_138-376delinsTG	XP_006719590.1:n.138-377_138-376delinsTG
XM_011538613.1:c.138-380_138-379delinsTG	XP_011536915.1:n.138-380_138-379delinsTG
NM_001330437.1:c.138-377_138-376delinsTG	NP_001317366.1:n.138-377_138-376delinsTG
NM_002834.4:c.138-377_138-376delinsTG	NP_002825.3:n.138-377_138-376delinsTG
NM_080601.2:c.138-377_138-376delinsTG	NP_542168.1:n.138-377_138-376delinsTG
XM_011538613.2:c.138-380_138-379delinsTG	XP_011536915.1:n.138-380_138-379delinsTG
XM_017019722.1:c.138-380_138-379delinsTG	XP_016875211.1:n.138-380_138-379delinsTG
NM_001330437.2:c.138-377_138-376delinsTG	NP_001317366.1:n.138-377_138-376delinsTG
NM_001374625.1:c.138-380_138-379delinsTG	NP_001361554.1:n.138-380_138-379delinsTG
NM_002834.5:c.138-377_138-376delinsTG MANE Select	NP_002825.3:n.138-377_138-376delinsTG
NM_080601.3:c.138-377_138-376delinsTG	NP_542168.1:n.138-377_138-376delinsTG