Canonical Allele Identifier: CA403381058
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090674T>A , CM000681.2:g.4090674T>A GRCh38
NC_000019.9:g.4090672T>A , CM000681.1:g.4090672T>A GRCh37
NC_000019.8:g.4041672T>A NCBI36
NG_007996.1:g.38455A>T , LRG_750:g.38455A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1566A>T
ENST00000688002.1:n.3278A>T
ENST00000688751.1:n.263A>T
ENST00000689792.1:n.1031A>T
ENST00000262948.10:c.1127A>T MANE Select ENSP00000262948.4:p.Glu376Val
ENST00000262948.9:c.1127A>T ENSP00000262948.3:p.Glu376Val
ENST00000394867.8:c.836A>T ENSP00000378336.1:p.Glu279Val
ENST00000597263.5:n.312A>T
ENST00000599021.1:c.237A>T
ENST00000600584.5:n.2576A>T
ENST00000601786.5:n.1428A>T
NM_030662.3:c.1127A>T , LRG_750t1:c.1127A>T NP_109587.1:p.Glu376Val
XM_006722799.2:c.848A>T XP_006722862.1:p.Glu283Val
XM_011528133.1:c.557A>T XP_011526435.1:p.Glu186Val
NM_030662.4:c.1127A>T MANE Select NP_109587.1:p.Glu376Val