Canonical Allele Identifier: CA2319219746
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090615_4090616delinsTG , CM000681.2:g.4090615_4090616delinsTG GRCh38
NC_000019.9:g.4090613_4090614delinsTG , CM000681.1:g.4090613_4090614delinsTG GRCh37
NC_000019.8:g.4041613_4041614delinsTG NCBI36
NG_007996.1:g.38513_38514delinsCA , LRG_750:g.38513_38514delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1624_1625delinsCA
ENST00000688002.1:n.3336_3337delinsCA
ENST00000688751.1:n.321_322delinsCA
ENST00000689792.1:n.1089_1090delinsCA
ENST00000262948.10:c.1185_1186delinsCA MANE Select ENSP00000262948.4:p.Pro395=
ENST00000262948.9:c.1185_1186delinsCA ENSP00000262948.3:p.Pro395=
ENST00000394867.8:c.894_895delinsCA ENSP00000378336.1:p.Pro298=
ENST00000597263.5:n.370_371delinsCA
ENST00000599021.1:c.295_296delinsCA
ENST00000600584.5:n.2634_2635delinsCA
ENST00000601786.5:n.1486_1487delinsCA
NM_030662.3:c.1185_1186delinsCA , LRG_750t1:c.1185_1186delinsCA NP_109587.1:p.Pro395=
XM_006722799.2:c.906_907delinsCA XP_006722862.1:p.Pro302=
XM_011528133.1:c.615_616delinsCA XP_011526435.1:p.Pro205=
NM_030662.4:c.1185_1186delinsCA MANE Select NP_109587.1:p.Pro395=
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