Canonical Allele Identifier: CA2319224236
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4098994_4098999delinsGACAGA , CM000681.2:g.4098994_4098999delinsGACAGA GRCh38
NC_000019.9:g.4098992_4098997delinsGACAGA , CM000681.1:g.4098992_4098997delinsGACAGA GRCh37
NC_000019.8:g.4049992_4049997delinsGACAGA NCBI36
NG_007996.1:g.30130_30135delinsTCTGTC , LRG_750:g.30130_30135delinsTCTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1358+202_1358+207delinsTCTGTC
ENST00000687128.1:n.1560_1565delinsTCTGTC
ENST00000688002.1:n.1415_1420delinsTCTGTC
ENST00000689792.1:n.823+202_823+207delinsTCTGTC
ENST00000262948.10:c.919+202_919+207delinsTCTGTC MANE Select ENSP00000262948.4:n.919+202_919+207delinsTCTGTC
ENST00000262948.9:c.919+202_919+207delinsTCTGTC ENSP00000262948.3:n.919+202_919+207delinsTCTGTC
ENST00000394867.8:c.628+202_628+207delinsTCTGTC ENSP00000378336.1:n.628+202_628+207delinsTCTGTC
ENST00000595715.1:n.734+202_734+207delinsTCTGTC
ENST00000597263.5:n.169+2020_169+2025delinsTCTGTC
ENST00000599021.1:c.30-1656_30-1651delinsTCTGTC
ENST00000600584.5:n.1479+202_1479+207delinsTCTGTC
ENST00000601786.5:n.1220+202_1220+207delinsTCTGTC
NM_030662.3:c.919+202_919+207delinsTCTGTC , LRG_750t1:c.919+202_919+207delinsTCTGTC NP_109587.1:n.919+202_919+207delinsTCTGTC
XM_006722799.2:c.705+2020_705+2025delinsTCTGTC XP_006722862.1:n.705+2020_705+2025delinsTCTGTC
XM_011528133.1:c.349+202_349+207delinsTCTGTC XP_011526435.1:n.349+202_349+207delinsTCTGTC
XM_017026989.1:c.919+202_919+207delinsTCTGTC XP_016882478.1:n.919+202_919+207delinsTCTGTC
XM_017026990.1:c.705+2020_705+2025delinsTCTGTC XP_016882479.1:n.705+2020_705+2025delinsTCTGTC
NM_030662.4:c.919+202_919+207delinsTCTGTC MANE Select NP_109587.1:n.919+202_919+207delinsTCTGTC