Canonical Allele Identifier: CA403380703
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2912384
ClinVar RCV Id: RCV003654840
gnomAD v4: 19-4090620-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090620G>A , CM000681.2:g.4090620G>A GRCh38
NC_000019.9:g.4090618G>A , CM000681.1:g.4090618G>A GRCh37
NC_000019.8:g.4041618G>A NCBI36
NG_007996.1:g.38509C>T , LRG_750:g.38509C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1620C>T
ENST00000688002.1:n.3332C>T
ENST00000688751.1:n.317C>T
ENST00000689792.1:n.1085C>T
ENST00000262948.10:c.1181C>T MANE Select ENSP00000262948.4:p.Thr394Ile
ENST00000262948.9:c.1181C>T ENSP00000262948.3:p.Thr394Ile
ENST00000394867.8:c.890C>T ENSP00000378336.1:p.Thr297Ile
ENST00000597263.5:n.366C>T
ENST00000599021.1:c.291C>T
ENST00000600584.5:n.2630C>T
ENST00000601786.5:n.1482C>T
NM_030662.3:c.1181C>T , LRG_750t1:c.1181C>T NP_109587.1:p.Thr394Ile
XM_006722799.2:c.902C>T XP_006722862.1:p.Thr301Ile
XM_011528133.1:c.611C>T XP_011526435.1:p.Thr204Ile
NM_030662.4:c.1181C>T MANE Select NP_109587.1:p.Thr394Ile