Canonical Allele Identifier: CA2319219815
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090751C= , CM000681.2:g.4090751C= GRCh38
NC_000019.9:g.4090749C= , CM000681.1:g.4090749C= GRCh37
NC_000019.8:g.4041749C= NCBI36
NG_007996.1:g.38378G= , LRG_750:g.38378G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-43G=
ENST00000688002.1:n.3244-43G=
ENST00000688751.1:n.229-43G=
ENST00000689792.1:n.997-43G=
ENST00000262948.10:c.1093-43G= MANE Select ENSP00000262948.4:n.1093-43G=
ENST00000262948.9:c.1093-43G= ENSP00000262948.3:n.1093-43G=
ENST00000394867.8:c.802-43G= ENSP00000378336.1:n.802-43G=
ENST00000597263.5:n.278-43G=
ENST00000599021.1:c.203-43G=
ENST00000600584.5:n.2542-43G=
ENST00000601786.5:n.1394-43G=
NM_030662.3:c.1093-43G= , LRG_750t1:c.1093-43G= NP_109587.1:n.1093-43G=
XM_006722799.2:c.814-43G= XP_006722862.1:n.814-43G=
XM_011528133.1:c.523-43G= XP_011526435.1:n.523-43G=
NM_030662.4:c.1093-43G= MANE Select NP_109587.1:n.1093-43G=
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