Canonical Allele Identifier: CA403380962
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090655A>G (hg19) chr19:g.4090657A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090657A>G , CM000681.2:g.4090657A>G GRCh38
NC_000019.9:g.4090655A>G , CM000681.1:g.4090655A>G GRCh37
NC_000019.8:g.4041655A>G NCBI36
NG_007996.1:g.38472T>C , LRG_750:g.38472T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1583T>C
ENST00000688002.1:n.3295T>C
ENST00000688751.1:n.280T>C
ENST00000689792.1:n.1048T>C
ENST00000262948.10:c.1144T>C MANE Select ENSP00000262948.4:p.Trp382Arg
ENST00000262948.9:c.1144T>C ENSP00000262948.3:p.Trp382Arg
ENST00000394867.8:c.853T>C ENSP00000378336.1:p.Trp285Arg
ENST00000597263.5:n.329T>C
ENST00000599021.1:c.254T>C
ENST00000600584.5:n.2593T>C
ENST00000601786.5:n.1445T>C
NM_030662.3:c.1144T>C , LRG_750t1:c.1144T>C NP_109587.1:p.Trp382Arg
XM_006722799.2:c.865T>C XP_006722862.1:p.Trp289Arg
XM_011528133.1:c.574T>C XP_011526435.1:p.Trp192Arg
NM_030662.4:c.1144T>C MANE Select NP_109587.1:p.Trp382Arg
Search 100 bp 5'
Search 100 bp 3'