Canonical Allele Identifier: CA2319219779
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090671A= , CM000681.2:g.4090671A= GRCh38
NC_000019.9:g.4090669A= , CM000681.1:g.4090669A= GRCh37
NC_000019.8:g.4041669A= NCBI36
NG_007996.1:g.38458T= , LRG_750:g.38458T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1569T=
ENST00000688002.1:n.3281T=
ENST00000688751.1:n.266T=
ENST00000689792.1:n.1034T=
ENST00000262948.10:c.1130T= MANE Select ENSP00000262948.4:p.Val377=
ENST00000262948.9:c.1130T= ENSP00000262948.3:p.Val377=
ENST00000394867.8:c.839T= ENSP00000378336.1:p.Val280=
ENST00000597263.5:n.315T=
ENST00000599021.1:c.240T=
ENST00000600584.5:n.2579T=
ENST00000601786.5:n.1431T=
NM_030662.3:c.1130T= , LRG_750t1:c.1130T= NP_109587.1:p.Val377=
XM_006722799.2:c.851T= XP_006722862.1:p.Val284=
XM_011528133.1:c.560T= XP_011526435.1:p.Val187=
NM_030662.4:c.1130T= MANE Select NP_109587.1:p.Val377=