Canonical Allele Identifier: CA2584876436
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090384_4090385del , CM000681.2:g.4090384_4090385del GRCh38
NC_000019.9:g.4090382_4090383del , CM000681.1:g.4090382_4090383del GRCh37
NC_000019.8:g.4041382_4041383del NCBI36
NG_007996.1:g.38750_38751del , LRG_750:g.38750_38751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1861_1862del
ENST00000688751.1:n.558_559del
ENST00000689792.1:n.1326_1327del
ENST00000262948.10:c.*219_*220del MANE Select ENSP00000262948.4:n.*219_*220del
ENST00000262948.9:c.*219_*220del ENSP00000262948.3:n.*219_*220del
ENST00000394867.8:c.*219_*220del ENSP00000378336.1:n.*219_*220del
ENST00000600584.5:n.2871_2872del
ENST00000601786.5:n.1723_1724del
NM_030662.3:c.*219_*220del , LRG_750t1:c.*219_*220del NP_109587.1:n.*219_*220del
XM_006722799.2:c.*219_*220del XP_006722862.1:n.*219_*220del
XM_011528133.1:c.*219_*220del XP_011526435.1:n.*219_*220del
NM_030662.4:c.*219_*220del MANE Select NP_109587.1:n.*219_*220del