Canonical Allele Identifier: CA2319219714
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090573_4090575delinsCGG , CM000681.2:g.4090573_4090575delinsCGG GRCh38
NC_000019.9:g.4090571_4090573delinsCGG , CM000681.1:g.4090571_4090573delinsCGG GRCh37
NC_000019.8:g.4041571_4041573delinsCGG NCBI36
NG_007996.1:g.38554_38556delinsCCG , LRG_750:g.38554_38556delinsCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1665_1667delinsCCG
ENST00000688002.1:n.3377_3379delinsCCG
ENST00000688751.1:n.362_364delinsCCG
ENST00000689792.1:n.1130_1132delinsCCG
ENST00000262948.10:c.*23_*25delinsCCG MANE Select ENSP00000262948.4:n.*23_*25delinsCCG
ENST00000262948.9:c.*23_*25delinsCCG ENSP00000262948.3:n.*23_*25delinsCCG
ENST00000394867.8:c.*23_*25delinsCCG ENSP00000378336.1:n.*23_*25delinsCCG
ENST00000597263.5:n.411_413delinsCCG
ENST00000600584.5:n.2675_2677delinsCCG
ENST00000601786.5:n.1527_1529delinsCCG
NM_030662.3:c.*23_*25delinsCCG , LRG_750t1:c.*23_*25delinsCCG NP_109587.1:n.*23_*25delinsCCG
XM_006722799.2:c.*23_*25delinsCCG XP_006722862.1:n.*23_*25delinsCCG
XM_011528133.1:c.*23_*25delinsCCG XP_011526435.1:n.*23_*25delinsCCG
NM_030662.4:c.*23_*25delinsCCG MANE Select NP_109587.1:n.*23_*25delinsCCG
Search 100 bp 5'
Search 100 bp 3'