Canonical Allele Identifier: CA504984317
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1987944
ClinVar RCV Id: RCV002781048
dbSNP Id: rs1181694893
gnomAD v2: 19-4090634-G-A
gnomAD v4: 19-4090636-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090636G>A , CM000681.2:g.4090636G>A GRCh38
NC_000019.9:g.4090634G>A , CM000681.1:g.4090634G>A GRCh37
NC_000019.8:g.4041634G>A NCBI36
NG_007996.1:g.38493C>T , LRG_750:g.38493C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1604C>T
ENST00000688002.1:n.3316C>T
ENST00000688751.1:n.301C>T
ENST00000689792.1:n.1069C>T
ENST00000262948.10:c.1165C>T MANE Select ENSP00000262948.4:p.Leu389=
ENST00000262948.9:c.1165C>T ENSP00000262948.3:p.Leu389=
ENST00000394867.8:c.874C>T ENSP00000378336.1:p.Leu292=
ENST00000597263.5:n.350C>T
ENST00000599021.1:c.275C>T
ENST00000600584.5:n.2614C>T
ENST00000601786.5:n.1466C>T
NM_030662.3:c.1165C>T , LRG_750t1:c.1165C>T NP_109587.1:p.Leu389=
XM_006722799.2:c.886C>T XP_006722862.1:p.Leu296=
XM_011528133.1:c.595C>T XP_011526435.1:p.Leu199=
NM_030662.4:c.1165C>T MANE Select NP_109587.1:p.Leu389=