Canonical Allele Identifier: CA2319219555
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090332_4090336delinsTCTCC , CM000681.2:g.4090332_4090336delinsTCTCC GRCh38
NC_000019.9:g.4090330_4090334delinsTCTCC , CM000681.1:g.4090330_4090334delinsTCTCC GRCh37
NC_000019.8:g.4041330_4041334delinsTCTCC NCBI36
NG_007996.1:g.38793_38797delinsGGAGA , LRG_750:g.38793_38797delinsGGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1369_1373delinsGGAGA
ENST00000262948.10:c.*262_*266delinsGGAGA MANE Select ENSP00000262948.4:n.*262_*266delinsGGAGA
ENST00000262948.9:c.*262_*266delinsGGAGA ENSP00000262948.3:n.*262_*266delinsGGAGA
ENST00000600584.5:n.2914_2918delinsGGAGA
ENST00000601786.5:n.1766_1770delinsGGAGA
NM_030662.3:c.*262_*266delinsGGAGA , LRG_750t1:c.*262_*266delinsGGAGA NP_109587.1:n.*262_*266delinsGGAGA
XM_006722799.2:c.*262_*266delinsGGAGA XP_006722862.1:n.*262_*266delinsGGAGA
XM_011528133.1:c.*262_*266delinsGGAGA XP_011526435.1:n.*262_*266delinsGGAGA
NM_030662.4:c.*262_*266delinsGGAGA MANE Select NP_109587.1:n.*262_*266delinsGGAGA
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