Canonical Allele Identifier: CA2319219614
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090419_4090420delinsAG , CM000681.2:g.4090419_4090420delinsAG GRCh38
NC_000019.9:g.4090417_4090418delinsAG , CM000681.1:g.4090417_4090418delinsAG GRCh37
NC_000019.8:g.4041417_4041418delinsAG NCBI36
NG_007996.1:g.38709_38710delinsCT , LRG_750:g.38709_38710delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1820_1821delinsCT
ENST00000688751.1:n.517_518delinsCT
ENST00000689792.1:n.1285_1286delinsCT
ENST00000262948.10:c.*178_*179delinsCT MANE Select ENSP00000262948.4:n.*178_*179delinsCT
ENST00000262948.9:c.*178_*179delinsCT ENSP00000262948.3:n.*178_*179delinsCT
ENST00000394867.8:c.*178_*179delinsCT ENSP00000378336.1:n.*178_*179delinsCT
ENST00000600584.5:n.2830_2831delinsCT
ENST00000601786.5:n.1682_1683delinsCT
NM_030662.3:c.*178_*179delinsCT , LRG_750t1:c.*178_*179delinsCT NP_109587.1:n.*178_*179delinsCT
XM_006722799.2:c.*178_*179delinsCT XP_006722862.1:n.*178_*179delinsCT
XM_011528133.1:c.*178_*179delinsCT XP_011526435.1:n.*178_*179delinsCT
NM_030662.4:c.*178_*179delinsCT MANE Select NP_109587.1:n.*178_*179delinsCT
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