Canonical Allele Identifier: CA2063741469

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489372G= , CM000674.2:g.112489372G=	GRCh38
NC_000012.11:g.112927176G= , CM000674.1:g.112927176G=	GRCh37
NC_000012.10:g.111411559G=	NCBI36
NG_007459.1:g.75641G= , LRG_614:g.75641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1599+197G=	ENSP00000491593.2:n.1599+197G=
ENST00000685487.1:c.*185G=	ENSP00000508503.1:n.*185G=
ENST00000687624.1:n.461G=
ENST00000687906.1:c.1485+197G=	ENSP00000509536.1:n.1485+197G=
ENST00000688597.1:c.1224+7167G=	ENSP00000510628.1:n.1224+7167G=
ENST00000688701.1:n.843+197G=
ENST00000690210.1:c.1599+197G=	ENSP00000509272.1:n.1599+197G=
ENST00000690472.1:n.808+197G=
ENST00000692624.1:c.*145+197G=	ENSP00000508953.1:n.*145+197G=
ENST00000351677.7:c.1599+197G= MANE Select	ENSP00000340944.3:n.1599+197G=
ENST00000351677.6:c.1599+197G=	ENSP00000340944.2:n.1599+197G=
ENST00000635625.1:c.1611+197G=	ENSP00000489597.1:n.1611+197G=
NM_002834.3:c.1599+197G= , LRG_614t1:c.1599+197G=	NP_002825.3:n.1599+197G=
XM_006719526.1:c.1611+197G=	XP_006719589.1:n.1611+197G=
XM_006719527.1:c.1497+197G=	XP_006719590.1:n.1497+197G=
XM_011538613.1:c.1608+197G=	XP_011536915.1:n.1608+197G=
NM_001330437.1:c.1611+197G=	NP_001317366.1:n.1611+197G=
NM_002834.4:c.1599+197G=	NP_002825.3:n.1599+197G=
XM_011538613.2:c.1608+197G=	XP_011536915.1:n.1608+197G=
XM_017019722.1:c.1596+197G=	XP_016875211.1:n.1596+197G=
NM_001330437.2:c.1611+197G=	NP_001317366.1:n.1611+197G=
NM_001374625.1:c.1596+197G=	NP_001361554.1:n.1596+197G=
NM_002834.5:c.1599+197G= MANE Select	NP_002825.3:n.1599+197G=