Canonical Allele Identifier: CA2319219599
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090399_4090400delinsTC , CM000681.2:g.4090399_4090400delinsTC GRCh38
NC_000019.9:g.4090397_4090398delinsTC , CM000681.1:g.4090397_4090398delinsTC GRCh37
NC_000019.8:g.4041397_4041398delinsTC NCBI36
NG_007996.1:g.38729_38730delinsGA , LRG_750:g.38729_38730delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1840_1841delinsGA
ENST00000688751.1:n.537_538delinsGA
ENST00000689792.1:n.1305_1306delinsGA
ENST00000262948.10:c.*198_*199delinsGA MANE Select ENSP00000262948.4:n.*198_*199delinsGA
ENST00000262948.9:c.*198_*199delinsGA ENSP00000262948.3:n.*198_*199delinsGA
ENST00000394867.8:c.*198_*199delinsGA ENSP00000378336.1:n.*198_*199delinsGA
ENST00000600584.5:n.2850_2851delinsGA
ENST00000601786.5:n.1702_1703delinsGA
NM_030662.3:c.*198_*199delinsGA , LRG_750t1:c.*198_*199delinsGA NP_109587.1:n.*198_*199delinsGA
XM_006722799.2:c.*198_*199delinsGA XP_006722862.1:n.*198_*199delinsGA
XM_011528133.1:c.*198_*199delinsGA XP_011526435.1:n.*198_*199delinsGA
NM_030662.4:c.*198_*199delinsGA MANE Select NP_109587.1:n.*198_*199delinsGA
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