Canonical Allele Identifier: CA657382350
Gene: MAP2K2 HGNC NCBI

Linked Data

COSMIC: COSN21064452
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090486_4090487insA , CM000681.2:g.4090486_4090487insA GRCh38
NC_000019.9:g.4090484_4090485insA , CM000681.1:g.4090484_4090485insA GRCh37
NC_000019.8:g.4041484_4041485insA NCBI36
NG_007996.1:g.38642_38643insT , LRG_750:g.38642_38643insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1753_1754insT
ENST00000688002.1:n.3465_3466insT
ENST00000688751.1:n.450_451insT
ENST00000689792.1:n.1218_1219insT
ENST00000262948.10:c.*111_*112insT MANE Select ENSP00000262948.4:n.*111_*112insT
ENST00000262948.9:c.*111_*112insT ENSP00000262948.3:n.*111_*112insT
ENST00000394867.8:c.*111_*112insT ENSP00000378336.1:n.*111_*112insT
ENST00000597263.5:n.499_500insT
ENST00000600584.5:n.2763_2764insT
ENST00000601786.5:n.1615_1616insT
NM_030662.3:c.*111_*112insT , LRG_750t1:c.*111_*112insT NP_109587.1:n.*111_*112insT
XM_006722799.2:c.*111_*112insT XP_006722862.1:n.*111_*112insT
XM_011528133.1:c.*111_*112insT XP_011526435.1:n.*111_*112insT
NM_030662.4:c.*111_*112insT MANE Select NP_109587.1:n.*111_*112insT
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