Canonical Allele Identifier: CA2584876421
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090357del , CM000681.2:g.4090357del GRCh38
NC_000019.9:g.4090355del , CM000681.1:g.4090355del GRCh37
NC_000019.8:g.4041355del NCBI36
NG_007996.1:g.38773del , LRG_750:g.38773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1884del
ENST00000688751.1:n.581del
ENST00000689792.1:n.1349del
ENST00000262948.10:c.*242del MANE Select ENSP00000262948.4:n.*242del
ENST00000262948.9:c.*242del ENSP00000262948.3:n.*242del
ENST00000394867.8:c.*242del ENSP00000378336.1:n.*242del
ENST00000600584.5:n.2894del
ENST00000601786.5:n.1746del
NM_030662.3:c.*242del , LRG_750t1:c.*242del NP_109587.1:n.*242del
XM_006722799.2:c.*242del XP_006722862.1:n.*242del
XM_011528133.1:c.*242del XP_011526435.1:n.*242del
NM_030662.4:c.*242del MANE Select NP_109587.1:n.*242del