Canonical Allele Identifier: CA2584876410
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090340-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090340T>A , CM000681.2:g.4090340T>A GRCh38
NC_000019.9:g.4090338T>A , CM000681.1:g.4090338T>A GRCh37
NC_000019.8:g.4041338T>A NCBI36
NG_007996.1:g.38789A>T , LRG_750:g.38789A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000688751.1:n.597A>T
ENST00000689792.1:n.1365A>T
ENST00000262948.10:c.*258A>T MANE Select ENSP00000262948.4:n.*258A>T
ENST00000262948.9:c.*258A>T ENSP00000262948.3:n.*258A>T
ENST00000394867.8:c.*258A>T ENSP00000378336.1:n.*258A>T
ENST00000600584.5:n.2910A>T
ENST00000601786.5:n.1762A>T
NM_030662.3:c.*258A>T , LRG_750t1:c.*258A>T NP_109587.1:n.*258A>T
XM_006722799.2:c.*258A>T XP_006722862.1:n.*258A>T
XM_011528133.1:c.*258A>T XP_011526435.1:n.*258A>T
NM_030662.4:c.*258A>T MANE Select NP_109587.1:n.*258A>T