Canonical Allele Identifier: CA2319224228
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4098982_4098983delinsGC , CM000681.2:g.4098982_4098983delinsGC GRCh38
NC_000019.9:g.4098980_4098981delinsGC , CM000681.1:g.4098980_4098981delinsGC GRCh37
NC_000019.8:g.4049980_4049981delinsGC NCBI36
NG_007996.1:g.30146_30147delinsGC , LRG_750:g.30146_30147delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1358+218_1358+219delinsGC
ENST00000687128.1:n.1576_1577delinsGC
ENST00000688002.1:n.1431_1432delinsGC
ENST00000689792.1:n.823+218_823+219delinsGC
ENST00000262948.10:c.919+218_919+219delinsGC MANE Select ENSP00000262948.4:n.919+218_919+219delinsGC
ENST00000262948.9:c.919+218_919+219delinsGC ENSP00000262948.3:n.919+218_919+219delinsGC
ENST00000394867.8:c.628+218_628+219delinsGC ENSP00000378336.1:n.628+218_628+219delinsGC
ENST00000595715.1:n.734+218_734+219delinsGC
ENST00000597263.5:n.169+2036_169+2037delinsGC
ENST00000599021.1:c.30-1640_30-1639delinsGC
ENST00000600584.5:n.1479+218_1479+219delinsGC
ENST00000601786.5:n.1220+218_1220+219delinsGC
NM_030662.3:c.919+218_919+219delinsGC , LRG_750t1:c.919+218_919+219delinsGC NP_109587.1:n.919+218_919+219delinsGC
XM_006722799.2:c.705+2036_705+2037delinsGC XP_006722862.1:n.705+2036_705+2037delinsGC
XM_011528133.1:c.349+218_349+219delinsGC XP_011526435.1:n.349+218_349+219delinsGC
XM_017026989.1:c.919+218_919+219delinsGC XP_016882478.1:n.919+218_919+219delinsGC
XM_017026990.1:c.705+2036_705+2037delinsGC XP_016882479.1:n.705+2036_705+2037delinsGC
NM_030662.4:c.919+218_919+219delinsGC MANE Select NP_109587.1:n.919+218_919+219delinsGC