Canonical Allele Identifier: CA683695381

Gene: PTPN11

Linked Data

• dbSNP Id: rs1174547956
• gnomAD v3: 12-112477596-GT-G
• gnomAD v4: 12-112477596-GT-G
• MyVariant Identifiers: chr12:g.112915401del (hg19) ; chr12:g.112477597del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112477602del , CM000674.2:g.112477602del	GRCh38
NC_000012.11:g.112915406del , CM000674.1:g.112915406del	GRCh37
NC_000012.10:g.111399789del	NCBI36
NG_007459.1:g.63871del , LRG_614:g.63871del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.854-49del	ENSP00000491593.2:n.854-49del
ENST00000685487.1:c.854-49del	ENSP00000508503.1:n.854-49del
ENST00000687906.1:c.740-49del	ENSP00000509536.1:n.740-49del
ENST00000688597.1:c.854-49del	ENSP00000510628.1:n.854-49del
ENST00000690210.1:c.854-49del	ENSP00000509272.1:n.854-49del
ENST00000692624.1:c.854-49del	ENSP00000508953.1:n.854-49del
ENST00000351677.7:c.854-49del MANE Select	ENSP00000340944.3:n.854-49del
ENST00000351677.6:c.854-49del	ENSP00000340944.2:n.854-49del
ENST00000392597.5:c.854-49del	ENSP00000376376.1:n.854-49del
ENST00000635625.1:c.854-49del	ENSP00000489597.1:n.854-49del
NM_002834.3:c.854-49del , LRG_614t1:c.854-49del	NP_002825.3:n.854-49del
NM_080601.1:c.854-49del	NP_542168.1:n.854-49del
XM_006719526.1:c.854-49del	XP_006719589.1:n.854-49del
XM_006719527.1:c.740-49del	XP_006719590.1:n.740-49del
XM_011538613.1:c.851-49del	XP_011536915.1:n.851-49del
NM_001330437.1:c.854-49del	NP_001317366.1:n.854-49del
NM_002834.4:c.854-49del	NP_002825.3:n.854-49del
NM_080601.2:c.854-49del	NP_542168.1:n.854-49del
XM_011538613.2:c.851-49del	XP_011536915.1:n.851-49del
XM_017019722.1:c.851-49del	XP_016875211.1:n.851-49del
NM_001330437.2:c.854-49del	NP_001317366.1:n.854-49del
NM_001374625.1:c.851-49del	NP_001361554.1:n.851-49del
NM_002834.5:c.854-49del MANE Select	NP_002825.3:n.854-49del
NM_080601.3:c.854-49del	NP_542168.1:n.854-49del