Canonical Allele Identifier: CA504984335
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1457657051

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090658G>A , CM000681.2:g.4090658G>A GRCh38
NC_000019.9:g.4090656G>A , CM000681.1:g.4090656G>A GRCh37
NC_000019.8:g.4041656G>A NCBI36
NG_007996.1:g.38471C>T , LRG_750:g.38471C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1582C>T
ENST00000688002.1:n.3294C>T
ENST00000688751.1:n.279C>T
ENST00000689792.1:n.1047C>T
ENST00000262948.10:c.1143C>T MANE Select ENSP00000262948.4:p.Gly381=
ENST00000262948.9:c.1143C>T ENSP00000262948.3:p.Gly381=
ENST00000394867.8:c.852C>T ENSP00000378336.1:p.Gly284=
ENST00000597263.5:n.328C>T
ENST00000599021.1:c.253C>T
ENST00000600584.5:n.2592C>T
ENST00000601786.5:n.1444C>T
NM_030662.3:c.1143C>T , LRG_750t1:c.1143C>T NP_109587.1:p.Gly381=
XM_006722799.2:c.864C>T XP_006722862.1:p.Gly288=
XM_011528133.1:c.573C>T XP_011526435.1:p.Gly191=
NM_030662.4:c.1143C>T MANE Select NP_109587.1:p.Gly381=