Canonical Allele Identifier: CA2576573113
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090561del , CM000681.2:g.4090561del GRCh38
NC_000019.9:g.4090559del , CM000681.1:g.4090559del GRCh37
NC_000019.8:g.4041559del NCBI36
NG_007996.1:g.38570del , LRG_750:g.38570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1681del
ENST00000688002.1:n.3393del
ENST00000688751.1:n.378del
ENST00000689792.1:n.1146del
ENST00000262948.10:c.*39del MANE Select ENSP00000262948.4:n.*39del
ENST00000262948.9:c.*39del ENSP00000262948.3:n.*39del
ENST00000394867.8:c.*39del ENSP00000378336.1:n.*39del
ENST00000597263.5:n.427del
ENST00000600584.5:n.2691del
ENST00000601786.5:n.1543del
NM_030662.3:c.*39del , LRG_750t1:c.*39del NP_109587.1:n.*39del
XM_006722799.2:c.*39del XP_006722862.1:n.*39del
XM_011528133.1:c.*39del XP_011526435.1:n.*39del
NM_030662.4:c.*39del MANE Select NP_109587.1:n.*39del