Canonical Allele Identifier: CA16607833
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 383208
ClinVar RCV Id: RCV000441365
dbSNP Id: rs1057521556
gnomAD v2: 19-4090594-T-A
gnomAD v4: 19-4090596-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090596T>A , CM000681.2:g.4090596T>A GRCh38
NC_000019.9:g.4090594T>A , CM000681.1:g.4090594T>A GRCh37
NC_000019.8:g.4041594T>A NCBI36
NG_007996.1:g.38533A>T , LRG_750:g.38533A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1644A>T
ENST00000688002.1:n.3356A>T
ENST00000688751.1:n.341A>T
ENST00000689792.1:n.1109A>T
ENST00000262948.10:c.*2A>T MANE Select ENSP00000262948.4:n.*2A>T
ENST00000262948.9:c.*2A>T ENSP00000262948.3:n.*2A>T
ENST00000394867.8:c.*2A>T ENSP00000378336.1:n.*2A>T
ENST00000597263.5:n.390A>T
ENST00000600584.5:n.2654A>T
ENST00000601786.5:n.1506A>T
NM_030662.3:c.*2A>T , LRG_750t1:c.*2A>T NP_109587.1:n.*2A>T
XM_006722799.2:c.*2A>T XP_006722862.1:n.*2A>T
XM_011528133.1:c.*2A>T XP_011526435.1:n.*2A>T
NM_030662.4:c.*2A>T MANE Select NP_109587.1:n.*2A>T