Canonical Allele Identifier: CA403381073
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2770949
ClinVar RCV Id: RCV003540449
gnomAD v4: 19-4090678-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090678C>A , CM000681.2:g.4090678C>A GRCh38
NC_000019.9:g.4090676C>A , CM000681.1:g.4090676C>A GRCh37
NC_000019.8:g.4041676C>A NCBI36
NG_007996.1:g.38451G>T , LRG_750:g.38451G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1562G>T
ENST00000688002.1:n.3274G>T
ENST00000688751.1:n.259G>T
ENST00000689792.1:n.1027G>T
ENST00000262948.10:c.1123G>T MANE Select ENSP00000262948.4:p.Glu375Ter
ENST00000262948.9:c.1123G>T ENSP00000262948.3:p.Glu375Ter
ENST00000394867.8:c.832G>T ENSP00000378336.1:p.Glu278Ter
ENST00000597263.5:n.308G>T
ENST00000599021.1:c.233G>T
ENST00000600584.5:n.2572G>T
ENST00000601786.5:n.1424G>T
NM_030662.3:c.1123G>T , LRG_750t1:c.1123G>T NP_109587.1:p.Glu375Ter
XM_006722799.2:c.844G>T XP_006722862.1:p.Glu282Ter
XM_011528133.1:c.553G>T XP_011526435.1:p.Glu185Ter
NM_030662.4:c.1123G>T MANE Select NP_109587.1:p.Glu375Ter