Canonical Allele Identifier: CA2063755212

Gene: PTPN11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112502045_112502049delinsTCTCC , CM000674.2:g.112502045_112502049delinsTCTCC	GRCh38
NC_000012.11:g.112939849_112939853delinsTCTCC , CM000674.1:g.112939849_112939853delinsTCTCC	GRCh37
NC_000012.10:g.111424232_111424236delinsTCTCC	NCBI36
NG_007459.1:g.88314_88318delinsTCTCC , LRG_614:g.88314_88318delinsTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1600-99_1600-95delinsTCTCC	ENSP00000491593.2:n.1600-99_1600-95delinsTCTCC
ENST00000685487.1:c.*802-99_*802-95delinsTCTCC	ENSP00000508503.1:n.*802-99_*802-95delinsTCTCC
ENST00000687120.1:n.884_888delinsTCTCC
ENST00000687906.1:c.1486-99_1486-95delinsTCTCC	ENSP00000509536.1:n.1486-99_1486-95delinsTCTCC
ENST00000688597.1:c.1225-99_1225-95delinsTCTCC	ENSP00000510628.1:n.1225-99_1225-95delinsTCTCC
ENST00000688701.1:n.844-99_844-95delinsTCTCC
ENST00000690210.1:c.1600-99_1600-95delinsTCTCC	ENSP00000509272.1:n.1600-99_1600-95delinsTCTCC
ENST00000690472.1:n.809-99_809-95delinsTCTCC
ENST00000692624.1:c.*146-99_*146-95delinsTCTCC	ENSP00000508953.1:n.*146-99_*146-95delinsTCTCC
ENST00000351677.7:c.1600-99_1600-95delinsTCTCC MANE Select	ENSP00000340944.3:n.1600-99_1600-95delinsTCTCC
ENST00000351677.6:c.1600-99_1600-95delinsTCTCC	ENSP00000340944.2:n.1600-99_1600-95delinsTCTCC
ENST00000635625.1:c.1612-99_1612-95delinsTCTCC	ENSP00000489597.1:n.1612-99_1612-95delinsTCTCC
NM_002834.3:c.1600-99_1600-95delinsTCTCC , LRG_614t1:c.1600-99_1600-95delinsTCTCC	NP_002825.3:n.1600-99_1600-95delinsTCTCC
XM_006719526.1:c.1612-99_1612-95delinsTCTCC	XP_006719589.1:n.1612-99_1612-95delinsTCTCC
XM_006719527.1:c.1498-99_1498-95delinsTCTCC	XP_006719590.1:n.1498-99_1498-95delinsTCTCC
XM_011538613.1:c.1609-99_1609-95delinsTCTCC	XP_011536915.1:n.1609-99_1609-95delinsTCTCC
NM_001330437.1:c.1612-99_1612-95delinsTCTCC	NP_001317366.1:n.1612-99_1612-95delinsTCTCC
NM_002834.4:c.1600-99_1600-95delinsTCTCC	NP_002825.3:n.1600-99_1600-95delinsTCTCC
XM_011538613.2:c.1609-99_1609-95delinsTCTCC	XP_011536915.1:n.1609-99_1609-95delinsTCTCC
XM_017019722.1:c.1597-99_1597-95delinsTCTCC	XP_016875211.1:n.1597-99_1597-95delinsTCTCC
NM_001330437.2:c.1612-99_1612-95delinsTCTCC	NP_001317366.1:n.1612-99_1612-95delinsTCTCC
NM_001374625.1:c.1597-99_1597-95delinsTCTCC	NP_001361554.1:n.1597-99_1597-95delinsTCTCC
NM_002834.5:c.1600-99_1600-95delinsTCTCC MANE Select	NP_002825.3:n.1600-99_1600-95delinsTCTCC