Canonical Allele Identifier: CA504984316
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 513229
dbSNP Id: rs1473228474
gnomAD v2: 19-4090632-C-T
gnomAD v3: 19-4090634-C-T
gnomAD v4: 19-4090634-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090634C>T , CM000681.2:g.4090634C>T GRCh38
NC_000019.9:g.4090632C>T , CM000681.1:g.4090632C>T GRCh37
NC_000019.8:g.4041632C>T NCBI36
NG_007996.1:g.38495G>A , LRG_750:g.38495G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1606G>A
ENST00000688002.1:n.3318G>A
ENST00000688751.1:n.303G>A
ENST00000689792.1:n.1071G>A
ENST00000262948.10:c.1167G>A MANE Select ENSP00000262948.4:p.Leu389=
ENST00000262948.9:c.1167G>A ENSP00000262948.3:p.Leu389=
ENST00000394867.8:c.876G>A ENSP00000378336.1:p.Leu292=
ENST00000597263.5:n.352G>A
ENST00000599021.1:c.277G>A
ENST00000600584.5:n.2616G>A
ENST00000601786.5:n.1468G>A
NM_030662.3:c.1167G>A , LRG_750t1:c.1167G>A NP_109587.1:p.Leu389=
XM_006722799.2:c.888G>A XP_006722862.1:p.Leu296=
XM_011528133.1:c.597G>A XP_011526435.1:p.Leu199=
NM_030662.4:c.1167G>A MANE Select NP_109587.1:p.Leu389=