Canonical Allele Identifier: CA2584877068
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094617_4094620del , CM000681.2:g.4094617_4094620del GRCh38
NC_000019.9:g.4094615_4094618del , CM000681.1:g.4094615_4094618del GRCh37
NC_000019.8:g.4045615_4045618del NCBI36
NG_007996.1:g.34509_34512del , LRG_750:g.34509_34512del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1486-122_1486-119del
ENST00000688002.1:n.3198-122_3198-119del
ENST00000688751.1:n.183-122_183-119del
ENST00000689792.1:n.951-122_951-119del
ENST00000262948.10:c.1047-122_1047-119del MANE Select ENSP00000262948.4:n.1047-122_1047-119del
ENST00000262948.9:c.1047-122_1047-119del ENSP00000262948.3:n.1047-122_1047-119del
ENST00000394867.8:c.756-122_756-119del ENSP00000378336.1:n.756-122_756-119del
ENST00000597263.5:n.232-122_232-119del
ENST00000599021.1:c.157-122_157-119del
ENST00000600584.5:n.2374_2377del
ENST00000601786.5:n.1348-122_1348-119del
NM_030662.3:c.1047-122_1047-119del , LRG_750t1:c.1047-122_1047-119del NP_109587.1:n.1047-122_1047-119del
XM_006722799.2:c.768-122_768-119del XP_006722862.1:n.768-122_768-119del
XM_011528133.1:c.477-122_477-119del XP_011526435.1:n.477-122_477-119del
XM_017026989.1:c.1473_1476del XP_016882478.1:p.Arg493GlufsTer?
XM_017026990.1:c.1194_1197del XP_016882479.1:p.Arg400GlufsTer?
NM_030662.4:c.1047-122_1047-119del MANE Select NP_109587.1:n.1047-122_1047-119del