Canonical Allele Identifier: CA403391514
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4110584G>T , CM000681.2:g.4110584G>T GRCh38
NC_000019.9:g.4110582G>T , CM000681.1:g.4110582G>T GRCh37
NC_000019.8:g.4061582G>T NCBI36
NG_007996.1:g.18545C>A , LRG_750:g.18545C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.814C>A
ENST00000687128.1:n.814C>A
ENST00000262948.10:c.375C>A MANE Select ENSP00000262948.4:p.Cys125Ter
ENST00000262948.9:c.375C>A ENSP00000262948.3:p.Cys125Ter
ENST00000394867.8:c.84C>A ENSP00000378336.1:p.Cys28Ter
ENST00000599345.1:n.572C>A
NM_030662.3:c.375C>A , LRG_750t1:c.375C>A NP_109587.1:p.Cys125Ter
XM_006722799.2:c.375C>A XP_006722862.1:p.Cys125Ter
XM_017026989.1:c.375C>A XP_016882478.1:p.Cys125Ter
XM_017026990.1:c.375C>A XP_016882479.1:p.Cys125Ter
XM_017026991.1:c.375C>A XP_016882480.1:p.Cys125Ter
NM_030662.4:c.375C>A MANE Select NP_109587.1:p.Cys125Ter
Search 100 bp 5'
Search 100 bp 3'