Canonical Allele Identifier: CA386779951

Gene: PTPN11

Linked Data

• MyVariant Identifiers: chr12:g.112926918T>C (hg19) ; chr12:g.112489114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112489114T>C , CM000674.2:g.112489114T>C	GRCh38
NC_000012.11:g.112926918T>C , CM000674.1:g.112926918T>C	GRCh37
NC_000012.10:g.111411301T>C	NCBI36
NG_007459.1:g.75383T>C , LRG_614:g.75383T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639857.2:c.1538T>C	ENSP00000491593.2:p.Phe513Ser
ENST00000685487.1:c.1538T>C	ENSP00000508503.1:p.Phe513Ser
ENST00000687624.1:n.203T>C
ENST00000687906.1:c.1424T>C	ENSP00000509536.1:p.Phe475Ser
ENST00000688597.1:c.1224+6909T>C	ENSP00000510628.1:n.1224+6909T>C
ENST00000688701.1:n.782T>C
ENST00000690210.1:c.1538T>C	ENSP00000509272.1:p.Phe513Ser
ENST00000690472.1:n.747T>C
ENST00000692624.1:c.*84T>C	ENSP00000508953.1:n.*84T>C
ENST00000351677.7:c.1538T>C MANE Select	ENSP00000340944.3:p.Phe513Ser
ENST00000351677.6:c.1538T>C	ENSP00000340944.2:p.Phe513Ser
ENST00000635625.1:c.1550T>C	ENSP00000489597.1:p.Phe517Ser
ENST00000635652.1:c.551T>C	ENSP00000489541.1:p.Phe184Ser
NM_002834.3:c.1538T>C , LRG_614t1:c.1538T>C	NP_002825.3:p.Phe513Ser
XM_006719526.1:c.1550T>C	XP_006719589.1:p.Phe517Ser
XM_006719527.1:c.1436T>C	XP_006719590.1:p.Phe479Ser
XM_011538613.1:c.1547T>C	XP_011536915.1:p.Phe516Ser
NM_001330437.1:c.1550T>C	NP_001317366.1:p.Phe517Ser
NM_002834.4:c.1538T>C	NP_002825.3:p.Phe513Ser
XM_011538613.2:c.1547T>C	XP_011536915.1:p.Phe516Ser
XM_017019722.1:c.1535T>C	XP_016875211.1:p.Phe512Ser
NM_001330437.2:c.1550T>C	NP_001317366.1:p.Phe517Ser
NM_001374625.1:c.1535T>C	NP_001361554.1:p.Phe512Ser
NM_002834.5:c.1538T>C MANE Select	NP_002825.3:p.Phe513Ser