Canonical Allele Identifier: CA607377547

Gene: PTPN11

Linked Data

• dbSNP Id: rs1180047898
• gnomAD v2: 12-112927000-A-G
• MyVariant Identifiers: chr12:g.112927000A>G (hg19) ; chr12:g.112489196A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489196A>G , CM000674.2:g.112489196A>G	GRCh38
NC_000012.11:g.112927000A>G , CM000674.1:g.112927000A>G	GRCh37
NC_000012.10:g.111411383A>G	NCBI36
NG_007459.1:g.75465A>G , LRG_614:g.75465A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1599+21A>G	ENSP00000491593.2:n.1599+21A>G
ENST00000685487.1:c.*9A>G	ENSP00000508503.1:n.*9A>G
ENST00000687624.1:n.285A>G
ENST00000687906.1:c.1485+21A>G	ENSP00000509536.1:n.1485+21A>G
ENST00000688597.1:c.1224+6991A>G	ENSP00000510628.1:n.1224+6991A>G
ENST00000688701.1:n.843+21A>G
ENST00000690210.1:c.1599+21A>G	ENSP00000509272.1:n.1599+21A>G
ENST00000690472.1:n.808+21A>G
ENST00000692624.1:c.*145+21A>G	ENSP00000508953.1:n.*145+21A>G
ENST00000351677.7:c.1599+21A>G MANE Select	ENSP00000340944.3:n.1599+21A>G
ENST00000351677.6:c.1599+21A>G	ENSP00000340944.2:n.1599+21A>G
ENST00000635625.1:c.1611+21A>G	ENSP00000489597.1:n.1611+21A>G
NM_002834.3:c.1599+21A>G , LRG_614t1:c.1599+21A>G	NP_002825.3:n.1599+21A>G
XM_006719526.1:c.1611+21A>G	XP_006719589.1:n.1611+21A>G
XM_006719527.1:c.1497+21A>G	XP_006719590.1:n.1497+21A>G
XM_011538613.1:c.1608+21A>G	XP_011536915.1:n.1608+21A>G
NM_001330437.1:c.1611+21A>G	NP_001317366.1:n.1611+21A>G
NM_002834.4:c.1599+21A>G	NP_002825.3:n.1599+21A>G
XM_011538613.2:c.1608+21A>G	XP_011536915.1:n.1608+21A>G
XM_017019722.1:c.1596+21A>G	XP_016875211.1:n.1596+21A>G
NM_001330437.2:c.1611+21A>G	NP_001317366.1:n.1611+21A>G
NM_001374625.1:c.1596+21A>G	NP_001361554.1:n.1596+21A>G
NM_002834.5:c.1599+21A>G MANE Select	NP_002825.3:n.1599+21A>G