Canonical Allele Identifier: CA683660511

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112418951T>A , CM000674.2:g.112418951T>A	GRCh38
NC_000012.11:g.112856755T>A , CM000674.1:g.112856755T>A	GRCh37
NC_000012.10:g.111341138T>A	NCBI36
NG_007459.1:g.5220T>A , LRG_614:g.5220T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.-161T>A	ENSP00000491593.2:n.-161T>A
ENST00000685487.1:c.-161T>A	ENSP00000508503.1:n.-161T>A
ENST00000687906.1:c.-161T>A	ENSP00000509536.1:n.-161T>A
ENST00000688597.1:c.-161T>A	ENSP00000510628.1:n.-161T>A
ENST00000690210.1:c.-161T>A	ENSP00000509272.1:n.-161T>A
ENST00000692624.1:c.-161T>A	ENSP00000508953.1:n.-161T>A
ENST00000351677.7:c.-161T>A MANE Select	ENSP00000340944.3:n.-161T>A
ENST00000351677.6:c.-161T>A	ENSP00000340944.2:n.-161T>A
ENST00000392597.5:c.-161T>A	ENSP00000376376.1:n.-161T>A
ENST00000531326.1:n.443T>A
NM_002834.3:c.-161T>A , LRG_614t1:c.-161T>A	NP_002825.3:n.-161T>A
NM_080601.1:c.-161T>A	NP_542168.1:n.-161T>A
XM_006719526.1:c.-161T>A	XP_006719589.1:n.-161T>A
XM_006719527.1:c.-161T>A	XP_006719590.1:n.-161T>A
XM_011538613.1:c.-161T>A	XP_011536915.1:n.-161T>A
NM_001330437.1:c.-161T>A	NP_001317366.1:n.-161T>A
NM_002834.4:c.-161T>A	NP_002825.3:n.-161T>A
NM_080601.2:c.-161T>A	NP_542168.1:n.-161T>A
XM_011538613.2:c.-161T>A	XP_011536915.1:n.-161T>A
XM_017019722.1:c.-161T>A	XP_016875211.1:n.-161T>A
NM_001330437.2:c.-161T>A	NP_001317366.1:n.-161T>A
NM_001374625.1:c.-161T>A	NP_001361554.1:n.-161T>A
NM_002834.5:c.-161T>A MANE Select	NP_002825.3:n.-161T>A
NM_080601.3:c.-161T>A	NP_542168.1:n.-161T>A