Canonical Allele Identifier: CA2621024669

Gene: PTPN11

Linked Data

• gnomAD v4: 12-112477926-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112477930del , CM000674.2:g.112477930del	GRCh38
NC_000012.11:g.112915734del , CM000674.1:g.112915734del	GRCh37
NC_000012.10:g.111400117del	NCBI36
NG_007459.1:g.64199del , LRG_614:g.64199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1007del	ENSP00000491593.2:p.Asn336ThrfsTer3
ENST00000685487.1:c.1007del	ENSP00000508503.1:p.Asn336ThrfsTer3
ENST00000687906.1:c.893del	ENSP00000509536.1:p.Asn298ThrfsTer3
ENST00000688597.1:c.1007del	ENSP00000510628.1:p.Asn336ThrfsTer3
ENST00000690210.1:c.1007del	ENSP00000509272.1:p.Asn336ThrfsTer3
ENST00000692624.1:c.1007del	ENSP00000508953.1:p.Asn336ThrfsTer3
ENST00000351677.7:c.1007del MANE Select	ENSP00000340944.3:p.Asn336ThrfsTer3
ENST00000351677.6:c.1007del	ENSP00000340944.2:p.Asn336ThrfsTer3
ENST00000392597.5:c.1007del	ENSP00000376376.1:p.Asn336ThrfsTer3
ENST00000635625.1:c.1007del	ENSP00000489597.1:p.Asn336ThrfsTer3
NM_002834.3:c.1007del , LRG_614t1:c.1007del	NP_002825.3:p.Asn336ThrfsTer3
NM_080601.1:c.1007del	NP_542168.1:p.Asn336ThrfsTer3
XM_006719526.1:c.1007del	XP_006719589.1:p.Asn336ThrfsTer3
XM_006719527.1:c.893del	XP_006719590.1:p.Asn298ThrfsTer3
XM_011538613.1:c.1004del	XP_011536915.1:p.Asn335ThrfsTer3
NM_001330437.1:c.1007del	NP_001317366.1:p.Asn336ThrfsTer3
NM_002834.4:c.1007del	NP_002825.3:p.Asn336ThrfsTer3
NM_080601.2:c.1007del	NP_542168.1:p.Asn336ThrfsTer3
XM_011538613.2:c.1004del	XP_011536915.1:p.Asn335ThrfsTer3
XM_017019722.1:c.1004del	XP_016875211.1:p.Asn335ThrfsTer3
NM_001330437.2:c.1007del	NP_001317366.1:p.Asn336ThrfsTer3
NM_001374625.1:c.1004del	NP_001361554.1:p.Asn335ThrfsTer3
NM_002834.5:c.1007del MANE Select	NP_002825.3:p.Asn336ThrfsTer3
NM_080601.3:c.1007del	NP_542168.1:p.Asn336ThrfsTer3