Canonical Allele Identifier: CA2063739492

Gene: PTPN11

Linked Data

• dbSNP Id: rs2038055282

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112449965_112449966insTCTTGG , CM000674.2:g.112449965_112449966insTCTTGG	GRCh38
NC_000012.11:g.112887769_112887770insTCTTGG , CM000674.1:g.112887769_112887770insTCTTGG	GRCh37
NC_000012.10:g.111372152_111372153insTCTTGG	NCBI36
NG_007459.1:g.36234_36235insTCTTGG , LRG_614:g.36234_36235insTCTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.138-353_138-352insTCTTGG	ENSP00000491593.2:n.138-353_138-352insTCTTGG
ENST00000685487.1:c.138-353_138-352insTCTTGG	ENSP00000508503.1:n.138-353_138-352insTCTTGG
ENST00000687906.1:c.138-353_138-352insTCTTGG	ENSP00000509536.1:n.138-353_138-352insTCTTGG
ENST00000688597.1:c.138-353_138-352insTCTTGG	ENSP00000510628.1:n.138-353_138-352insTCTTGG
ENST00000690210.1:c.138-353_138-352insTCTTGG	ENSP00000509272.1:n.138-353_138-352insTCTTGG
ENST00000692624.1:c.138-353_138-352insTCTTGG	ENSP00000508953.1:n.138-353_138-352insTCTTGG
ENST00000351677.7:c.138-353_138-352insTCTTGG MANE Select	ENSP00000340944.3:n.138-353_138-352insTCTTGG
ENST00000639857.1:c.138-353_138-352insTCTTGG	ENSP00000491593.1:n.138-353_138-352insTCTTGG
ENST00000351677.6:c.138-353_138-352insTCTTGG	ENSP00000340944.2:n.138-353_138-352insTCTTGG
ENST00000392597.5:c.138-353_138-352insTCTTGG	ENSP00000376376.1:n.138-353_138-352insTCTTGG
ENST00000635625.1:c.138-353_138-352insTCTTGG	ENSP00000489597.1:n.138-353_138-352insTCTTGG
NM_002834.3:c.138-353_138-352insTCTTGG , LRG_614t1:c.138-353_138-352insTCTTGG	NP_002825.3:n.138-353_138-352insTCTTGG
NM_080601.1:c.138-353_138-352insTCTTGG	NP_542168.1:n.138-353_138-352insTCTTGG
XM_006719526.1:c.138-353_138-352insTCTTGG	XP_006719589.1:n.138-353_138-352insTCTTGG
XM_006719527.1:c.138-353_138-352insTCTTGG	XP_006719590.1:n.138-353_138-352insTCTTGG
XM_011538613.1:c.138-356_138-355insTCTTGG	XP_011536915.1:n.138-356_138-355insTCTTGG
NM_001330437.1:c.138-353_138-352insTCTTGG	NP_001317366.1:n.138-353_138-352insTCTTGG
NM_002834.4:c.138-353_138-352insTCTTGG	NP_002825.3:n.138-353_138-352insTCTTGG
NM_080601.2:c.138-353_138-352insTCTTGG	NP_542168.1:n.138-353_138-352insTCTTGG
XM_011538613.2:c.138-356_138-355insTCTTGG	XP_011536915.1:n.138-356_138-355insTCTTGG
XM_017019722.1:c.138-356_138-355insTCTTGG	XP_016875211.1:n.138-356_138-355insTCTTGG
NM_001330437.2:c.138-353_138-352insTCTTGG	NP_001317366.1:n.138-353_138-352insTCTTGG
NM_001374625.1:c.138-356_138-355insTCTTGG	NP_001361554.1:n.138-356_138-355insTCTTGG
NM_002834.5:c.138-353_138-352insTCTTGG MANE Select	NP_002825.3:n.138-353_138-352insTCTTGG
NM_080601.3:c.138-353_138-352insTCTTGG	NP_542168.1:n.138-353_138-352insTCTTGG