Canonical Allele Identifier: CA16042862

Gene: PTPN11

Linked Data

• ClinVar Variation Id: 372590
• ClinVar RCV Id: RCV000413720 ; RCV001201204
• dbSNP Id: rs397507507
• COSMIC: COSM13010
• MyVariant Identifiers: chr12:g.112888162G>C (hg19) ; chr12:g.112450358G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112450358G>C , CM000674.2:g.112450358G>C	GRCh38
NC_000012.11:g.112888162G>C , CM000674.1:g.112888162G>C	GRCh37
NC_000012.10:g.111372545G>C	NCBI36
NG_007459.1:g.36627G>C , LRG_614:g.36627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.178G>C	ENSP00000491593.2:p.Gly60Arg
ENST00000685487.1:c.178G>C	ENSP00000508503.1:p.Gly60Arg
ENST00000687906.1:c.178G>C	ENSP00000509536.1:p.Gly60Arg
ENST00000688597.1:c.178G>C	ENSP00000510628.1:p.Gly60Arg
ENST00000690210.1:c.178G>C	ENSP00000509272.1:p.Gly60Arg
ENST00000692624.1:c.178G>C	ENSP00000508953.1:p.Gly60Arg
ENST00000351677.7:c.178G>C MANE Select	ENSP00000340944.3:p.Gly60Arg
ENST00000639857.1:c.178G>C	ENSP00000491593.1:p.Gly60Arg
ENST00000351677.6:c.178G>C	ENSP00000340944.2:p.Gly60Arg
ENST00000392597.5:c.178G>C	ENSP00000376376.1:p.Gly60Arg
ENST00000635625.1:c.178G>C	ENSP00000489597.1:p.Gly60Arg
NM_002834.3:c.178G>C , LRG_614t1:c.178G>C	NP_002825.3:p.Gly60Arg
NM_080601.1:c.178G>C	NP_542168.1:p.Gly60Arg
XM_006719526.1:c.178G>C	XP_006719589.1:p.Gly60Arg
XM_006719527.1:c.178G>C	XP_006719590.1:p.Gly60Arg
XM_011538613.1:c.175G>C	XP_011536915.1:p.Gly59Arg
NM_001330437.1:c.178G>C	NP_001317366.1:p.Gly60Arg
NM_002834.4:c.178G>C	NP_002825.3:p.Gly60Arg
NM_080601.2:c.178G>C	NP_542168.1:p.Gly60Arg
XM_011538613.2:c.175G>C	XP_011536915.1:p.Gly59Arg
XM_017019722.1:c.175G>C	XP_016875211.1:p.Gly59Arg
NM_001330437.2:c.178G>C	NP_001317366.1:p.Gly60Arg
NM_001374625.1:c.175G>C	NP_001361554.1:p.Gly59Arg
NM_002834.5:c.178G>C MANE Select	NP_002825.3:p.Gly60Arg
NM_080601.3:c.178G>C	NP_542168.1:p.Gly60Arg