Canonical Allele Identifier: CA2584877182
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094734_4094741del , CM000681.2:g.4094734_4094741del GRCh38
NC_000019.9:g.4094732_4094739del , CM000681.1:g.4094732_4094739del GRCh37
NC_000019.8:g.4045732_4045739del NCBI36
NG_007996.1:g.34394_34401del , LRG_750:g.34394_34401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1486-237_1486-230del
ENST00000688002.1:n.3198-237_3198-230del
ENST00000688751.1:n.183-237_183-230del
ENST00000689792.1:n.951-237_951-230del
ENST00000262948.10:c.1047-237_1047-230del MANE Select ENSP00000262948.4:n.1047-237_1047-230del
ENST00000262948.9:c.1047-237_1047-230del ENSP00000262948.3:n.1047-237_1047-230del
ENST00000394867.8:c.756-237_756-230del ENSP00000378336.1:n.756-237_756-230del
ENST00000597263.5:n.232-237_232-230del
ENST00000599021.1:c.157-237_157-230del
ENST00000600584.5:n.2259_2266del
ENST00000601786.5:n.1348-237_1348-230del
NM_030662.3:c.1047-237_1047-230del , LRG_750t1:c.1047-237_1047-230del NP_109587.1:n.1047-237_1047-230del
XM_006722799.2:c.768-237_768-230del XP_006722862.1:n.768-237_768-230del
XM_011528133.1:c.477-237_477-230del XP_011526435.1:n.477-237_477-230del
XM_017026989.1:c.1358_1365del XP_016882478.1:p.Phe453SerfsTer?
XM_017026990.1:c.1079_1086del XP_016882479.1:p.Phe360SerfsTer?
NM_030662.4:c.1047-237_1047-230del MANE Select NP_109587.1:n.1047-237_1047-230del