Canonical Allele Identifier: CA2542875511

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112477894_112477895insG , CM000674.2:g.112477894_112477895insG	GRCh38
NC_000012.11:g.112915698_112915699insG , CM000674.1:g.112915698_112915699insG	GRCh37
NC_000012.10:g.111400081_111400082insG	NCBI36
NG_007459.1:g.64163_64164insG , LRG_614:g.64163_64164insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.971_972insG	ENSP00000491593.2:p.Ser326GlufsTer15
ENST00000685487.1:c.971_972insG	ENSP00000508503.1:p.Ser326GlufsTer15
ENST00000687906.1:c.857_858insG	ENSP00000509536.1:p.Ser288GlufsTer15
ENST00000688597.1:c.971_972insG	ENSP00000510628.1:p.Ser326GlufsTer15
ENST00000690210.1:c.971_972insG	ENSP00000509272.1:p.Ser326GlufsTer15
ENST00000692624.1:c.971_972insG	ENSP00000508953.1:p.Ser326GlufsTer15
ENST00000351677.7:c.971_972insG MANE Select	ENSP00000340944.3:p.Ser326GlufsTer15
ENST00000351677.6:c.971_972insG	ENSP00000340944.2:p.Ser326GlufsTer15
ENST00000392597.5:c.971_972insG	ENSP00000376376.1:p.Ser326GlufsTer15
ENST00000635625.1:c.971_972insG	ENSP00000489597.1:p.Ser326GlufsTer15
NM_002834.3:c.971_972insG , LRG_614t1:c.971_972insG	NP_002825.3:p.Ser326GlufsTer15
NM_080601.1:c.971_972insG	NP_542168.1:p.Ser326GlufsTer15
XM_006719526.1:c.971_972insG	XP_006719589.1:p.Ser326GlufsTer15
XM_006719527.1:c.857_858insG	XP_006719590.1:p.Ser288GlufsTer15
XM_011538613.1:c.968_969insG	XP_011536915.1:p.Ser325GlufsTer15
NM_001330437.1:c.971_972insG	NP_001317366.1:p.Ser326GlufsTer15
NM_002834.4:c.971_972insG	NP_002825.3:p.Ser326GlufsTer15
NM_080601.2:c.971_972insG	NP_542168.1:p.Ser326GlufsTer15
XM_011538613.2:c.968_969insG	XP_011536915.1:p.Ser325GlufsTer15
XM_017019722.1:c.968_969insG	XP_016875211.1:p.Ser325GlufsTer15
NM_001330437.2:c.971_972insG	NP_001317366.1:p.Ser326GlufsTer15
NM_001374625.1:c.968_969insG	NP_001361554.1:p.Ser325GlufsTer15
NM_002834.5:c.971_972insG MANE Select	NP_002825.3:p.Ser326GlufsTer15
NM_080601.3:c.971_972insG	NP_542168.1:p.Ser326GlufsTer15