Canonical Allele Identifier: CA386778096

Gene: PTPN11

Linked Data

• dbSNP Id: rs121918468
• MyVariant Identifiers: chr12:g.112926248G>C (hg19) ; chr12:g.112488444G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112488444G>C , CM000674.2:g.112488444G>C	GRCh38
NC_000012.11:g.112926248G>C , CM000674.1:g.112926248G>C	GRCh37
NC_000012.10:g.111410631G>C	NCBI36
NG_007459.1:g.74713G>C , LRG_614:g.74713G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000639857.2:c.1381G>C	ENSP00000491593.2:p.Ala461Pro
ENST00000685487.1:c.1381G>C	ENSP00000508503.1:p.Ala461Pro
ENST00000687624.1:n.46G>C
ENST00000687906.1:c.1267G>C	ENSP00000509536.1:p.Ala423Pro
ENST00000688597.1:c.1224+6239G>C	ENSP00000510628.1:n.1224+6239G>C
ENST00000688701.1:n.625G>C
ENST00000690210.1:c.1381G>C	ENSP00000509272.1:p.Ala461Pro
ENST00000690472.1:n.590G>C
ENST00000692624.1:c.1380-580G>C	ENSP00000508953.1:n.1380-580G>C
ENST00000351677.7:c.1381G>C MANE Select	ENSP00000340944.3:p.Ala461Pro
ENST00000351677.6:c.1381G>C	ENSP00000340944.2:p.Ala461Pro
ENST00000635625.1:c.1393G>C	ENSP00000489597.1:p.Ala465Pro
ENST00000635652.1:c.394G>C	ENSP00000489541.1:p.Ala132Pro
NM_002834.3:c.1381G>C , LRG_614t1:c.1381G>C	NP_002825.3:p.Ala461Pro
XM_006719526.1:c.1393G>C	XP_006719589.1:p.Ala465Pro
XM_006719527.1:c.1279G>C	XP_006719590.1:p.Ala427Pro
XM_011538613.1:c.1390G>C	XP_011536915.1:p.Ala464Pro
NM_001330437.1:c.1393G>C	NP_001317366.1:p.Ala465Pro
NM_002834.4:c.1381G>C	NP_002825.3:p.Ala461Pro
XM_011538613.2:c.1390G>C	XP_011536915.1:p.Ala464Pro
XM_017019722.1:c.1378G>C	XP_016875211.1:p.Ala460Pro
NM_001330437.2:c.1393G>C	NP_001317366.1:p.Ala465Pro
NM_001374625.1:c.1378G>C	NP_001361554.1:p.Ala460Pro
NM_002834.5:c.1381G>C MANE Select	NP_002825.3:p.Ala461Pro