Canonical Allele Identifier: CA2813356106
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090334_4090335dup , CM000681.2:g.4090334_4090335dup GRCh38
NC_000019.9:g.4090332_4090333dup , CM000681.1:g.4090332_4090333dup GRCh37
NC_000019.8:g.4041332_4041333dup NCBI36
NG_007996.1:g.38798_38799dup , LRG_750:g.38798_38799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1374_1375dup
ENST00000262948.10:c.*267_*268dup MANE Select ENSP00000262948.4:n.*267_*268dup
ENST00000262948.9:c.*267_*268dup ENSP00000262948.3:n.*267_*268dup
ENST00000600584.5:n.2919_2920dup
ENST00000601786.5:n.1771_1772dup
NM_030662.3:c.*267_*268dup , LRG_750t1:c.*267_*268dup NP_109587.1:n.*267_*268dup
XM_006722799.2:c.*267_*268dup XP_006722862.1:n.*267_*268dup
XM_011528133.1:c.*267_*268dup XP_011526435.1:n.*267_*268dup
NM_030662.4:c.*267_*268dup MANE Select NP_109587.1:n.*267_*268dup