Canonical Allele Identifier: CA2735512601
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2145036683
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090708_4090709insTGTGAG , CM000681.2:g.4090708_4090709insTGTGAG GRCh38
NC_000019.9:g.4090706_4090707insTGTGAG , CM000681.1:g.4090706_4090707insTGTGAG GRCh37
NC_000019.8:g.4041706_4041707insTGTGAG NCBI36
NG_007996.1:g.38420_38421insCTCACA , LRG_750:g.38420_38421insCTCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-1_1532insCTCACA
ENST00000688002.1:n.3244-1_3244insCTCACA
ENST00000688751.1:n.229-1_229insCTCACA
ENST00000689792.1:n.997-1_997insCTCACA
ENST00000262948.10:c.1093-1_1093insCTCACA MANE Select ENSP00000262948.4:n.1093-1_1093insCTCACA
ENST00000262948.9:c.1093-1_1093insCTCACA ENSP00000262948.3:n.1093-1_1093insCTCACA
ENST00000394867.8:c.802-1_802insCTCACA ENSP00000378336.1:n.802-1_802insCTCACA
ENST00000597263.5:n.278-1_278insCTCACA
ENST00000599021.1:c.203-1_203insCTCACA
ENST00000600584.5:n.2542-1_2542insCTCACA
ENST00000601786.5:n.1394-1_1394insCTCACA
NM_030662.3:c.1093-1_1093insCTCACA , LRG_750t1:c.1093-1_1093insCTCACA NP_109587.1:n.1093-1_1093insCTCACA
XM_006722799.2:c.814-1_814insCTCACA XP_006722862.1:n.814-1_814insCTCACA
XM_011528133.1:c.523-1_523insCTCACA XP_011526435.1:n.523-1_523insCTCACA
NM_030662.4:c.1093-1_1093insCTCACA MANE Select NP_109587.1:n.1093-1_1093insCTCACA
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