Canonical Allele Identifier: CA2319219760
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090638C= , CM000681.2:g.4090638C= GRCh38
NC_000019.9:g.4090636C= , CM000681.1:g.4090636C= GRCh37
NC_000019.8:g.4041636C= NCBI36
NG_007996.1:g.38491G= , LRG_750:g.38491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1602G=
ENST00000688002.1:n.3314G=
ENST00000688751.1:n.299G=
ENST00000689792.1:n.1067G=
ENST00000262948.10:c.1163G= MANE Select ENSP00000262948.4:p.Arg388=
ENST00000262948.9:c.1163G= ENSP00000262948.3:p.Arg388=
ENST00000394867.8:c.872G= ENSP00000378336.1:p.Arg291=
ENST00000597263.5:n.348G=
ENST00000599021.1:c.273G=
ENST00000600584.5:n.2612G=
ENST00000601786.5:n.1464G=
NM_030662.3:c.1163G= , LRG_750t1:c.1163G= NP_109587.1:p.Arg388=
XM_006722799.2:c.884G= XP_006722862.1:p.Arg295=
XM_011528133.1:c.593G= XP_011526435.1:p.Arg198=
NM_030662.4:c.1163G= MANE Select NP_109587.1:p.Arg388=