Canonical Allele Identifier: CA882241165
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1264571851

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090414del , CM000681.2:g.4090414del GRCh38
NC_000019.9:g.4090412del , CM000681.1:g.4090412del GRCh37
NC_000019.8:g.4041412del NCBI36
NG_007996.1:g.38718del , LRG_750:g.38718del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1829del
ENST00000688751.1:n.526del
ENST00000689792.1:n.1294del
ENST00000262948.10:c.*187del MANE Select ENSP00000262948.4:n.*187del
ENST00000262948.9:c.*187del ENSP00000262948.3:n.*187del
ENST00000394867.8:c.*187del ENSP00000378336.1:n.*187del
ENST00000600584.5:n.2839del
ENST00000601786.5:n.1691del
NM_030662.3:c.*187del , LRG_750t1:c.*187del NP_109587.1:n.*187del
XM_006722799.2:c.*187del XP_006722862.1:n.*187del
XM_011528133.1:c.*187del XP_011526435.1:n.*187del
NM_030662.4:c.*187del MANE Select NP_109587.1:n.*187del