Canonical Allele Identifier: CA2621024736

Gene: PTPN11

Linked Data

• gnomAD v4: 12-112478108-G-GCTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112478111_112478114dup , CM000674.2:g.112478111_112478114dup	GRCh38
NC_000012.11:g.112915915_112915918dup , CM000674.1:g.112915915_112915918dup	GRCh37
NC_000012.10:g.111400298_111400301dup	NCBI36
NG_007459.1:g.64380_64383dup , LRG_614:g.64380_64383dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1092+96_1092+99dup	ENSP00000491593.2:n.1092+96_1092+99dup
ENST00000685487.1:c.1092+96_1092+99dup	ENSP00000508503.1:n.1092+96_1092+99dup
ENST00000687906.1:c.978+96_978+99dup	ENSP00000509536.1:n.978+96_978+99dup
ENST00000688597.1:c.1092+96_1092+99dup	ENSP00000510628.1:n.1092+96_1092+99dup
ENST00000690210.1:c.1092+96_1092+99dup	ENSP00000509272.1:n.1092+96_1092+99dup
ENST00000692624.1:c.1092+96_1092+99dup	ENSP00000508953.1:n.1092+96_1092+99dup
ENST00000351677.7:c.1092+96_1092+99dup MANE Select	ENSP00000340944.3:n.1092+96_1092+99dup
ENST00000351677.6:c.1092+96_1092+99dup	ENSP00000340944.2:n.1092+96_1092+99dup
ENST00000392597.5:c.1092+96_1092+99dup	ENSP00000376376.1:n.1092+96_1092+99dup
ENST00000635625.1:c.1092+96_1092+99dup	ENSP00000489597.1:n.1092+96_1092+99dup
ENST00000635652.1:c.84+96_84+99dup	ENSP00000489541.1:n.84+96_84+99dup
NM_002834.3:c.1092+96_1092+99dup , LRG_614t1:c.1092+96_1092+99dup	NP_002825.3:n.1092+96_1092+99dup
NM_080601.1:c.1092+96_1092+99dup	NP_542168.1:n.1092+96_1092+99dup
XM_006719526.1:c.1092+96_1092+99dup	XP_006719589.1:n.1092+96_1092+99dup
XM_006719527.1:c.978+96_978+99dup	XP_006719590.1:n.978+96_978+99dup
XM_011538613.1:c.1089+96_1089+99dup	XP_011536915.1:n.1089+96_1089+99dup
NM_001330437.1:c.1092+96_1092+99dup	NP_001317366.1:n.1092+96_1092+99dup
NM_002834.4:c.1092+96_1092+99dup	NP_002825.3:n.1092+96_1092+99dup
NM_080601.2:c.1092+96_1092+99dup	NP_542168.1:n.1092+96_1092+99dup
XM_011538613.2:c.1089+96_1089+99dup	XP_011536915.1:n.1089+96_1089+99dup
XM_017019722.1:c.1089+96_1089+99dup	XP_016875211.1:n.1089+96_1089+99dup
NM_001330437.2:c.1092+96_1092+99dup	NP_001317366.1:n.1092+96_1092+99dup
NM_001374625.1:c.1089+96_1089+99dup	NP_001361554.1:n.1089+96_1089+99dup
NM_002834.5:c.1092+96_1092+99dup MANE Select	NP_002825.3:n.1092+96_1092+99dup
NM_080601.3:c.1092+96_1092+99dup	NP_542168.1:n.1092+96_1092+99dup