Canonical Allele Identifier: CA386779864

Gene: PTPN11

Linked Data

• dbSNP Id: rs1379175668
• MyVariant Identifiers: chr12:g.112926892G>T (hg19) ; chr12:g.112489088G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489088G>T , CM000674.2:g.112489088G>T	GRCh38
NC_000012.11:g.112926892G>T , CM000674.1:g.112926892G>T	GRCh37
NC_000012.10:g.111411275G>T	NCBI36
NG_007459.1:g.75357G>T , LRG_614:g.75357G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1512G>T	ENSP00000491593.2:p.Met504Ile
ENST00000685487.1:c.1512G>T	ENSP00000508503.1:p.Met504Ile
ENST00000687624.1:n.177G>T
ENST00000687906.1:c.1398G>T	ENSP00000509536.1:p.Met466Ile
ENST00000688597.1:c.1224+6883G>T	ENSP00000510628.1:n.1224+6883G>T
ENST00000688701.1:n.756G>T
ENST00000690210.1:c.1512G>T	ENSP00000509272.1:p.Met504Ile
ENST00000690472.1:n.721G>T
ENST00000692624.1:c.*58G>T	ENSP00000508953.1:n.*58G>T
ENST00000351677.7:c.1512G>T MANE Select	ENSP00000340944.3:p.Met504Ile
ENST00000351677.6:c.1512G>T	ENSP00000340944.2:p.Met504Ile
ENST00000635625.1:c.1524G>T	ENSP00000489597.1:p.Met508Ile
ENST00000635652.1:c.525G>T	ENSP00000489541.1:p.Met175Ile
NM_002834.3:c.1512G>T , LRG_614t1:c.1512G>T	NP_002825.3:p.Met504Ile
XM_006719526.1:c.1524G>T	XP_006719589.1:p.Met508Ile
XM_006719527.1:c.1410G>T	XP_006719590.1:p.Met470Ile
XM_011538613.1:c.1521G>T	XP_011536915.1:p.Met507Ile
NM_001330437.1:c.1524G>T	NP_001317366.1:p.Met508Ile
NM_002834.4:c.1512G>T	NP_002825.3:p.Met504Ile
XM_011538613.2:c.1521G>T	XP_011536915.1:p.Met507Ile
XM_017019722.1:c.1509G>T	XP_016875211.1:p.Met503Ile
NM_001330437.2:c.1524G>T	NP_001317366.1:p.Met508Ile
NM_001374625.1:c.1509G>T	NP_001361554.1:p.Met503Ile
NM_002834.5:c.1512G>T MANE Select	NP_002825.3:p.Met504Ile