Canonical Allele Identifier: CA481882119

Gene: PTPN11

Linked Data

• MyVariant Identifiers: chr12:g.112926856A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489052A>G , CM000674.2:g.112489052A>G	GRCh38
NC_000012.11:g.112926856A>G , CM000674.1:g.112926856A>G	GRCh37
NC_000012.10:g.111411239A>G	NCBI36
NG_007459.1:g.75321A>G , LRG_614:g.75321A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1476A>G	ENSP00000491593.2:p.Lys492=
ENST00000685487.1:c.1476A>G	ENSP00000508503.1:p.Lys492=
ENST00000687624.1:n.141A>G
ENST00000687906.1:c.1362A>G	ENSP00000509536.1:p.Lys454=
ENST00000688597.1:c.1224+6847A>G	ENSP00000510628.1:n.1224+6847A>G
ENST00000688701.1:n.720A>G
ENST00000690210.1:c.1476A>G	ENSP00000509272.1:p.Lys492=
ENST00000690472.1:n.685A>G
ENST00000692624.1:c.*22A>G	ENSP00000508953.1:n.*22A>G
ENST00000351677.7:c.1476A>G MANE Select	ENSP00000340944.3:p.Lys492=
ENST00000351677.6:c.1476A>G	ENSP00000340944.2:p.Lys492=
ENST00000635625.1:c.1488A>G	ENSP00000489597.1:p.Lys496=
ENST00000635652.1:c.489A>G	ENSP00000489541.1:p.Lys163=
NM_002834.3:c.1476A>G , LRG_614t1:c.1476A>G	NP_002825.3:p.Lys492=
XM_006719526.1:c.1488A>G	XP_006719589.1:p.Lys496=
XM_006719527.1:c.1374A>G	XP_006719590.1:p.Lys458=
XM_011538613.1:c.1485A>G	XP_011536915.1:p.Lys495=
NM_001330437.1:c.1488A>G	NP_001317366.1:p.Lys496=
NM_002834.4:c.1476A>G	NP_002825.3:p.Lys492=
XM_011538613.2:c.1485A>G	XP_011536915.1:p.Lys495=
XM_017019722.1:c.1473A>G	XP_016875211.1:p.Lys491=
NM_001330437.2:c.1488A>G	NP_001317366.1:p.Lys496=
NM_001374625.1:c.1473A>G	NP_001361554.1:p.Lys491=
NM_002834.5:c.1476A>G MANE Select	NP_002825.3:p.Lys492=