Canonical Allele Identifier: CA2576573117
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090573del , CM000681.2:g.4090573del GRCh38
NC_000019.9:g.4090571del , CM000681.1:g.4090571del GRCh37
NC_000019.8:g.4041571del NCBI36
NG_007996.1:g.38556del , LRG_750:g.38556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1667del
ENST00000688002.1:n.3379del
ENST00000688751.1:n.364del
ENST00000689792.1:n.1132del
ENST00000262948.10:c.*25del MANE Select ENSP00000262948.4:n.*25del
ENST00000262948.9:c.*25del ENSP00000262948.3:n.*25del
ENST00000394867.8:c.*25del ENSP00000378336.1:n.*25del
ENST00000597263.5:n.413del
ENST00000600584.5:n.2677del
ENST00000601786.5:n.1529del
NM_030662.3:c.*25del , LRG_750t1:c.*25del NP_109587.1:n.*25del
XM_006722799.2:c.*25del XP_006722862.1:n.*25del
XM_011528133.1:c.*25del XP_011526435.1:n.*25del
NM_030662.4:c.*25del MANE Select NP_109587.1:n.*25del
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