Canonical Allele Identifier: CA2584876507
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090442_4090443dup , CM000681.2:g.4090442_4090443dup GRCh38
NC_000019.9:g.4090440_4090441dup , CM000681.1:g.4090440_4090441dup GRCh37
NC_000019.8:g.4041440_4041441dup NCBI36
NG_007996.1:g.38689_38690dup , LRG_750:g.38689_38690dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1800_1801dup
ENST00000688751.1:n.497_498dup
ENST00000689792.1:n.1265_1266dup
ENST00000262948.10:c.*158_*159dup MANE Select ENSP00000262948.4:n.*158_*159dup
ENST00000262948.9:c.*158_*159dup ENSP00000262948.3:n.*158_*159dup
ENST00000394867.8:c.*158_*159dup ENSP00000378336.1:n.*158_*159dup
ENST00000597263.5:n.546_547dup
ENST00000600584.5:n.2810_2811dup
ENST00000601786.5:n.1662_1663dup
NM_030662.3:c.*158_*159dup , LRG_750t1:c.*158_*159dup NP_109587.1:n.*158_*159dup
XM_006722799.2:c.*158_*159dup XP_006722862.1:n.*158_*159dup
XM_011528133.1:c.*158_*159dup XP_011526435.1:n.*158_*159dup
NM_030662.4:c.*158_*159dup MANE Select NP_109587.1:n.*158_*159dup