Canonical Allele Identifier: CA2063775989

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112477994G= , CM000674.2:g.112477994G=	GRCh38
NC_000012.11:g.112915798G= , CM000674.1:g.112915798G=	GRCh37
NC_000012.10:g.111400181G=	NCBI36
NG_007459.1:g.64263G= , LRG_614:g.64263G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000639857.2:c.1071G=	ENSP00000491593.2:p.Thr357=
ENST00000685487.1:c.1071G=	ENSP00000508503.1:p.Thr357=
ENST00000687906.1:c.957G=	ENSP00000509536.1:p.Thr319=
ENST00000688597.1:c.1071G=	ENSP00000510628.1:p.Thr357=
ENST00000690210.1:c.1071G=	ENSP00000509272.1:p.Thr357=
ENST00000692624.1:c.1071G=	ENSP00000508953.1:p.Thr357=
ENST00000351677.7:c.1071G= MANE Select	ENSP00000340944.3:p.Thr357=
ENST00000351677.6:c.1071G=	ENSP00000340944.2:p.Thr357=
ENST00000392597.5:c.1071G=	ENSP00000376376.1:p.Thr357=
ENST00000635625.1:c.1071G=	ENSP00000489597.1:p.Thr357=
ENST00000635652.1:c.63G=	ENSP00000489541.1:p.Thr21=
NM_002834.3:c.1071G= , LRG_614t1:c.1071G=	NP_002825.3:p.Thr357=
NM_080601.1:c.1071G=	NP_542168.1:p.Thr357=
XM_006719526.1:c.1071G=	XP_006719589.1:p.Thr357=
XM_006719527.1:c.957G=	XP_006719590.1:p.Thr319=
XM_011538613.1:c.1068G=	XP_011536915.1:p.Thr356=
NM_001330437.1:c.1071G=	NP_001317366.1:p.Thr357=
NM_002834.4:c.1071G=	NP_002825.3:p.Thr357=
NM_080601.2:c.1071G=	NP_542168.1:p.Thr357=
XM_011538613.2:c.1068G=	XP_011536915.1:p.Thr356=
XM_017019722.1:c.1068G=	XP_016875211.1:p.Thr356=
NM_001330437.2:c.1071G=	NP_001317366.1:p.Thr357=
NM_001374625.1:c.1068G=	NP_001361554.1:p.Thr356=
NM_002834.5:c.1071G= MANE Select	NP_002825.3:p.Thr357=
NM_080601.3:c.1071G=	NP_542168.1:p.Thr357=