Canonical Allele Identifier: CA2319219775
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090661G= , CM000681.2:g.4090661G= GRCh38
NC_000019.9:g.4090659G= , CM000681.1:g.4090659G= GRCh37
NC_000019.8:g.4041659G= NCBI36
NG_007996.1:g.38468C= , LRG_750:g.38468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1579C=
ENST00000688002.1:n.3291C=
ENST00000688751.1:n.276C=
ENST00000689792.1:n.1044C=
ENST00000262948.10:c.1140C= MANE Select ENSP00000262948.4:p.Ala380=
ENST00000262948.9:c.1140C= ENSP00000262948.3:p.Ala380=
ENST00000394867.8:c.849C= ENSP00000378336.1:p.Ala283=
ENST00000597263.5:n.325C=
ENST00000599021.1:c.250C=
ENST00000600584.5:n.2589C=
ENST00000601786.5:n.1441C=
NM_030662.3:c.1140C= , LRG_750t1:c.1140C= NP_109587.1:p.Ala380=
XM_006722799.2:c.861C= XP_006722862.1:p.Ala287=
XM_011528133.1:c.570C= XP_011526435.1:p.Ala190=
NM_030662.4:c.1140C= MANE Select NP_109587.1:p.Ala380=