Canonical Allele Identifier: CA2319219741
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090611C= , CM000681.2:g.4090611C= GRCh38
NC_000019.9:g.4090609C= , CM000681.1:g.4090609C= GRCh37
NC_000019.8:g.4041609C= NCBI36
NG_007996.1:g.38518G= , LRG_750:g.38518G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1629G=
ENST00000688002.1:n.3341G=
ENST00000688751.1:n.326G=
ENST00000689792.1:n.1094G=
ENST00000262948.10:c.1190G= MANE Select ENSP00000262948.4:p.Arg397=
ENST00000262948.9:c.1190G= ENSP00000262948.3:p.Arg397=
ENST00000394867.8:c.899G= ENSP00000378336.1:p.Arg300=
ENST00000597263.5:n.375G=
ENST00000599021.1:c.300G=
ENST00000600584.5:n.2639G=
ENST00000601786.5:n.1491G=
NM_030662.3:c.1190G= , LRG_750t1:c.1190G= NP_109587.1:p.Arg397=
XM_006722799.2:c.911G= XP_006722862.1:p.Arg304=
XM_011528133.1:c.620G= XP_011526435.1:p.Arg207=
NM_030662.4:c.1190G= MANE Select NP_109587.1:p.Arg397=