Canonical Allele Identifier: CA2319219607
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090410_4090411delinsAC , CM000681.2:g.4090410_4090411delinsAC GRCh38
NC_000019.9:g.4090408_4090409delinsAC , CM000681.1:g.4090408_4090409delinsAC GRCh37
NC_000019.8:g.4041408_4041409delinsAC NCBI36
NG_007996.1:g.38718_38719delinsGT , LRG_750:g.38718_38719delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1829_1830delinsGT
ENST00000688751.1:n.526_527delinsGT
ENST00000689792.1:n.1294_1295delinsGT
ENST00000262948.10:c.*187_*188delinsGT MANE Select ENSP00000262948.4:n.*187_*188delinsGT
ENST00000262948.9:c.*187_*188delinsGT ENSP00000262948.3:n.*187_*188delinsGT
ENST00000394867.8:c.*187_*188delinsGT ENSP00000378336.1:n.*187_*188delinsGT
ENST00000600584.5:n.2839_2840delinsGT
ENST00000601786.5:n.1691_1692delinsGT
NM_030662.3:c.*187_*188delinsGT , LRG_750t1:c.*187_*188delinsGT NP_109587.1:n.*187_*188delinsGT
XM_006722799.2:c.*187_*188delinsGT XP_006722862.1:n.*187_*188delinsGT
XM_011528133.1:c.*187_*188delinsGT XP_011526435.1:n.*187_*188delinsGT
NM_030662.4:c.*187_*188delinsGT MANE Select NP_109587.1:n.*187_*188delinsGT
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