Canonical Allele Identifier: CA2319219785
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090688C= , CM000681.2:g.4090688C= GRCh38
NC_000019.9:g.4090686C= , CM000681.1:g.4090686C= GRCh37
NC_000019.8:g.4041686C= NCBI36
NG_007996.1:g.38441G= , LRG_750:g.38441G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1552G=
ENST00000688002.1:n.3264G=
ENST00000688751.1:n.249G=
ENST00000689792.1:n.1017G=
ENST00000262948.10:c.1113G= MANE Select ENSP00000262948.4:p.Arg371=
ENST00000262948.9:c.1113G= ENSP00000262948.3:p.Arg371=
ENST00000394867.8:c.822G= ENSP00000378336.1:p.Arg274=
ENST00000597263.5:n.298G=
ENST00000599021.1:c.223G=
ENST00000600584.5:n.2562G=
ENST00000601786.5:n.1414G=
NM_030662.3:c.1113G= , LRG_750t1:c.1113G= NP_109587.1:p.Arg371=
XM_006722799.2:c.834G= XP_006722862.1:p.Arg278=
XM_011528133.1:c.543G= XP_011526435.1:p.Arg181=
NM_030662.4:c.1113G= MANE Select NP_109587.1:p.Arg371=