Canonical Allele Identifier: CA2584876529
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090466dup , CM000681.2:g.4090466dup GRCh38
NC_000019.9:g.4090464dup , CM000681.1:g.4090464dup GRCh37
NC_000019.8:g.4041464dup NCBI36
NG_007996.1:g.38666dup , LRG_750:g.38666dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1777dup
ENST00000688002.1:n.3489dup
ENST00000688751.1:n.474dup
ENST00000689792.1:n.1242dup
ENST00000262948.10:c.*135dup MANE Select ENSP00000262948.4:n.*135dup
ENST00000262948.9:c.*135dup ENSP00000262948.3:n.*135dup
ENST00000394867.8:c.*135dup ENSP00000378336.1:n.*135dup
ENST00000597263.5:n.523dup
ENST00000600584.5:n.2787dup
ENST00000601786.5:n.1639dup
NM_030662.3:c.*135dup , LRG_750t1:c.*135dup NP_109587.1:n.*135dup
XM_006722799.2:c.*135dup XP_006722862.1:n.*135dup
XM_011528133.1:c.*135dup XP_011526435.1:n.*135dup
NM_030662.4:c.*135dup MANE Select NP_109587.1:n.*135dup