Canonical Allele Identifier: CA2621026824

Gene: PTPN11

Linked Data

• gnomAD v4: 12-112489326-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489327_112489328insTT , CM000674.2:g.112489327_112489328insTT	GRCh38
NC_000012.11:g.112927131_112927132insTT , CM000674.1:g.112927131_112927132insTT	GRCh37
NC_000012.10:g.111411514_111411515insTT	NCBI36
NG_007459.1:g.75596_75597insTT , LRG_614:g.75596_75597insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1599+152_1599+153insTT	ENSP00000491593.2:n.1599+152_1599+153insTT
ENST00000685487.1:c.*140_*141insTT	ENSP00000508503.1:n.*140_*141insTT
ENST00000687624.1:n.416_417insTT
ENST00000687906.1:c.1485+152_1485+153insTT	ENSP00000509536.1:n.1485+152_1485+153insTT
ENST00000688597.1:c.1224+7122_1224+7123insTT	ENSP00000510628.1:n.1224+7122_1224+7123insTT
ENST00000688701.1:n.843+152_843+153insTT
ENST00000690210.1:c.1599+152_1599+153insTT	ENSP00000509272.1:n.1599+152_1599+153insTT
ENST00000690472.1:n.808+152_808+153insTT
ENST00000692624.1:c.*145+152_*145+153insTT	ENSP00000508953.1:n.*145+152_*145+153insTT
ENST00000351677.7:c.1599+152_1599+153insTT MANE Select	ENSP00000340944.3:n.1599+152_1599+153insTT
ENST00000351677.6:c.1599+152_1599+153insTT	ENSP00000340944.2:n.1599+152_1599+153insTT
ENST00000635625.1:c.1611+152_1611+153insTT	ENSP00000489597.1:n.1611+152_1611+153insTT
NM_002834.3:c.1599+152_1599+153insTT , LRG_614t1:c.1599+152_1599+153insTT	NP_002825.3:n.1599+152_1599+153insTT
XM_006719526.1:c.1611+152_1611+153insTT	XP_006719589.1:n.1611+152_1611+153insTT
XM_006719527.1:c.1497+152_1497+153insTT	XP_006719590.1:n.1497+152_1497+153insTT
XM_011538613.1:c.1608+152_1608+153insTT	XP_011536915.1:n.1608+152_1608+153insTT
NM_001330437.1:c.1611+152_1611+153insTT	NP_001317366.1:n.1611+152_1611+153insTT
NM_002834.4:c.1599+152_1599+153insTT	NP_002825.3:n.1599+152_1599+153insTT
XM_011538613.2:c.1608+152_1608+153insTT	XP_011536915.1:n.1608+152_1608+153insTT
XM_017019722.1:c.1596+152_1596+153insTT	XP_016875211.1:n.1596+152_1596+153insTT
NM_001330437.2:c.1611+152_1611+153insTT	NP_001317366.1:n.1611+152_1611+153insTT
NM_001374625.1:c.1596+152_1596+153insTT	NP_001361554.1:n.1596+152_1596+153insTT
NM_002834.5:c.1599+152_1599+153insTT MANE Select	NP_002825.3:n.1599+152_1599+153insTT