Canonical Allele Identifier: CA683698324

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112508614A>G , CM000674.2:g.112508614A>G	GRCh38
NC_000012.11:g.112946418A>G , CM000674.1:g.112946418A>G	GRCh37
NC_000012.10:g.111430801A>G	NCBI36
NG_007459.1:g.94883A>G , LRG_614:g.94883A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685487.1:c.*3806A>G	ENSP00000508503.1:n.*3806A>G
ENST00000687120.1:n.6425A>G
ENST00000687906.1:c.*2822A>G	ENSP00000509536.1:n.*2822A>G
ENST00000688597.1:c.*2822A>G	ENSP00000510628.1:n.*2822A>G
ENST00000688701.1:n.3848A>G
ENST00000690210.1:c.*2822A>G	ENSP00000509272.1:n.*2822A>G
ENST00000690472.1:n.3813A>G
ENST00000692624.1:c.*3150A>G	ENSP00000508953.1:n.*3150A>G
ENST00000351677.7:c.*2822A>G MANE Select	ENSP00000340944.3:n.*2822A>G
ENST00000351677.6:c.*2822A>G	ENSP00000340944.2:n.*2822A>G
NM_002834.3:c.*2822A>G , LRG_614t1:c.*2822A>G	NP_002825.3:n.*2822A>G
XM_006719526.1:c.*2822A>G	XP_006719589.1:n.*2822A>G
XM_006719527.1:c.*2822A>G	XP_006719590.1:n.*2822A>G
XM_011538613.1:c.*2822A>G	XP_011536915.1:n.*2822A>G
NM_001330437.1:c.*2822A>G	NP_001317366.1:n.*2822A>G
NM_002834.4:c.*2822A>G	NP_002825.3:n.*2822A>G
XM_011538613.2:c.*2822A>G	XP_011536915.1:n.*2822A>G
XM_017019722.1:c.*2822A>G	XP_016875211.1:n.*2822A>G
NM_001330437.2:c.*2822A>G	NP_001317366.1:n.*2822A>G
NM_001374625.1:c.*2822A>G	NP_001361554.1:n.*2822A>G
NM_002834.5:c.*2822A>G MANE Select	NP_002825.3:n.*2822A>G