Canonical Allele Identifier: CA2319219651
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090465_4090467delinsCCG , CM000681.2:g.4090465_4090467delinsCCG GRCh38
NC_000019.9:g.4090463_4090465delinsCCG , CM000681.1:g.4090463_4090465delinsCCG GRCh37
NC_000019.8:g.4041463_4041465delinsCCG NCBI36
NG_007996.1:g.38662_38664delinsCGG , LRG_750:g.38662_38664delinsCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1773_1775delinsCGG
ENST00000688002.1:n.3485_3487delinsCGG
ENST00000688751.1:n.470_472delinsCGG
ENST00000689792.1:n.1238_1240delinsCGG
ENST00000262948.10:c.*131_*133delinsCGG MANE Select ENSP00000262948.4:n.*131_*133delinsCGG
ENST00000262948.9:c.*131_*133delinsCGG ENSP00000262948.3:n.*131_*133delinsCGG
ENST00000394867.8:c.*131_*133delinsCGG ENSP00000378336.1:n.*131_*133delinsCGG
ENST00000597263.5:n.519_521delinsCGG
ENST00000600584.5:n.2783_2785delinsCGG
ENST00000601786.5:n.1635_1637delinsCGG
NM_030662.3:c.*131_*133delinsCGG , LRG_750t1:c.*131_*133delinsCGG NP_109587.1:n.*131_*133delinsCGG
XM_006722799.2:c.*131_*133delinsCGG XP_006722862.1:n.*131_*133delinsCGG
XM_011528133.1:c.*131_*133delinsCGG XP_011526435.1:n.*131_*133delinsCGG
NM_030662.4:c.*131_*133delinsCGG MANE Select NP_109587.1:n.*131_*133delinsCGG
Search 100 bp 5'
Search 100 bp 3'