Canonical Allele Identifier: CA304445557
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs149035656

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090337_4090338del , CM000681.2:g.4090337_4090338del GRCh38
NC_000019.9:g.4090335_4090336del , CM000681.1:g.4090335_4090336del GRCh37
NC_000019.8:g.4041335_4041336del NCBI36
NG_007996.1:g.38791_38792del , LRG_750:g.38791_38792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1367_1368del
ENST00000262948.10:c.*260_*261del MANE Select ENSP00000262948.4:n.*260_*261del
ENST00000262948.9:c.*260_*261del ENSP00000262948.3:n.*260_*261del
ENST00000394867.8:c.*260_*261del ENSP00000378336.1:n.*260_*261del
ENST00000600584.5:n.2912_2913del
ENST00000601786.5:n.1764_1765del
NM_030662.3:c.*260_*261del , LRG_750t1:c.*260_*261del NP_109587.1:n.*260_*261del
XM_006722799.2:c.*260_*261del XP_006722862.1:n.*260_*261del
XM_011528133.1:c.*260_*261del XP_011526435.1:n.*260_*261del
NM_030662.4:c.*260_*261del MANE Select NP_109587.1:n.*260_*261del