Canonical Allele Identifier: CA2727239122

Gene: PTPN11

Linked Data

• dbSNP Id: rs2135915902

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112488987C>A , CM000674.2:g.112488987C>A	GRCh38
NC_000012.11:g.112926791C>A , CM000674.1:g.112926791C>A	GRCh37
NC_000012.10:g.111411174C>A	NCBI36
NG_007459.1:g.75256C>A , LRG_614:g.75256C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000639857.2:c.1448-37C>A	ENSP00000491593.2:n.1448-37C>A
ENST00000685487.1:c.1448-37C>A	ENSP00000508503.1:n.1448-37C>A
ENST00000687624.1:n.113-37C>A
ENST00000687906.1:c.1334-37C>A	ENSP00000509536.1:n.1334-37C>A
ENST00000688597.1:c.1224+6782C>A	ENSP00000510628.1:n.1224+6782C>A
ENST00000688701.1:n.692-37C>A
ENST00000690210.1:c.1448-37C>A	ENSP00000509272.1:n.1448-37C>A
ENST00000690472.1:n.657-37C>A
ENST00000692624.1:c.1380-37C>A	ENSP00000508953.1:n.1380-37C>A
ENST00000351677.7:c.1448-37C>A MANE Select	ENSP00000340944.3:n.1448-37C>A
ENST00000351677.6:c.1448-37C>A	ENSP00000340944.2:n.1448-37C>A
ENST00000635625.1:c.1460-37C>A	ENSP00000489597.1:n.1460-37C>A
ENST00000635652.1:c.461-37C>A	ENSP00000489541.1:n.461-37C>A
NM_002834.3:c.1448-37C>A , LRG_614t1:c.1448-37C>A	NP_002825.3:n.1448-37C>A
XM_006719526.1:c.1460-37C>A	XP_006719589.1:n.1460-37C>A
XM_006719527.1:c.1346-37C>A	XP_006719590.1:n.1346-37C>A
XM_011538613.1:c.1457-37C>A	XP_011536915.1:n.1457-37C>A
NM_001330437.1:c.1460-37C>A	NP_001317366.1:n.1460-37C>A
NM_002834.4:c.1448-37C>A	NP_002825.3:n.1448-37C>A
XM_011538613.2:c.1457-37C>A	XP_011536915.1:n.1457-37C>A
XM_017019722.1:c.1445-37C>A	XP_016875211.1:n.1445-37C>A
NM_001330437.2:c.1460-37C>A	NP_001317366.1:n.1460-37C>A
NM_001374625.1:c.1445-37C>A	NP_001361554.1:n.1445-37C>A
NM_002834.5:c.1448-37C>A MANE Select	NP_002825.3:n.1448-37C>A