Canonical Allele Identifier: CA403381066
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090674T>A (hg19) chr19:g.4090676T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090676T>A , CM000681.2:g.4090676T>A GRCh38
NC_000019.9:g.4090674T>A , CM000681.1:g.4090674T>A GRCh37
NC_000019.8:g.4041674T>A NCBI36
NG_007996.1:g.38453A>T , LRG_750:g.38453A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1564A>T
ENST00000688002.1:n.3276A>T
ENST00000688751.1:n.261A>T
ENST00000689792.1:n.1029A>T
ENST00000262948.10:c.1125A>T MANE Select ENSP00000262948.4:p.Glu375Asp
ENST00000262948.9:c.1125A>T ENSP00000262948.3:p.Glu375Asp
ENST00000394867.8:c.834A>T ENSP00000378336.1:p.Glu278Asp
ENST00000597263.5:n.310A>T
ENST00000599021.1:c.235A>T
ENST00000600584.5:n.2574A>T
ENST00000601786.5:n.1426A>T
NM_030662.3:c.1125A>T , LRG_750t1:c.1125A>T NP_109587.1:p.Glu375Asp
XM_006722799.2:c.846A>T XP_006722862.1:p.Glu282Asp
XM_011528133.1:c.555A>T XP_011526435.1:p.Glu185Asp
NM_030662.4:c.1125A>T MANE Select NP_109587.1:p.Glu375Asp
Search 100 bp 5'
Search 100 bp 3'