Canonical Allele Identifier: CA304445718
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs866048999
gnomAD v4: 19-4090684-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090684C>A , CM000681.2:g.4090684C>A GRCh38
NC_000019.9:g.4090682C>A , CM000681.1:g.4090682C>A GRCh37
NC_000019.8:g.4041682C>A NCBI36
NG_007996.1:g.38445G>T , LRG_750:g.38445G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1556G>T
ENST00000688002.1:n.3268G>T
ENST00000688751.1:n.253G>T
ENST00000689792.1:n.1021G>T
ENST00000262948.10:c.1117G>T MANE Select ENSP00000262948.4:p.Glu373Ter
ENST00000262948.9:c.1117G>T ENSP00000262948.3:p.Glu373Ter
ENST00000394867.8:c.826G>T ENSP00000378336.1:p.Glu276Ter
ENST00000597263.5:n.302G>T
ENST00000599021.1:c.227G>T
ENST00000600584.5:n.2566G>T
ENST00000601786.5:n.1418G>T
NM_030662.3:c.1117G>T , LRG_750t1:c.1117G>T NP_109587.1:p.Glu373Ter
XM_006722799.2:c.838G>T XP_006722862.1:p.Glu280Ter
XM_011528133.1:c.547G>T XP_011526435.1:p.Glu183Ter
NM_030662.4:c.1117G>T MANE Select NP_109587.1:p.Glu373Ter