Canonical Allele Identifier: CA2319219818
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090758A= , CM000681.2:g.4090758A= GRCh38
NC_000019.9:g.4090756A= , CM000681.1:g.4090756A= GRCh37
NC_000019.8:g.4041756A= NCBI36
NG_007996.1:g.38371T= , LRG_750:g.38371T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-50T=
ENST00000688002.1:n.3244-50T=
ENST00000688751.1:n.229-50T=
ENST00000689792.1:n.997-50T=
ENST00000262948.10:c.1093-50T= MANE Select ENSP00000262948.4:n.1093-50T=
ENST00000262948.9:c.1093-50T= ENSP00000262948.3:n.1093-50T=
ENST00000394867.8:c.802-50T= ENSP00000378336.1:n.802-50T=
ENST00000597263.5:n.278-50T=
ENST00000599021.1:c.203-50T=
ENST00000600584.5:n.2542-50T=
ENST00000601786.5:n.1394-50T=
NM_030662.3:c.1093-50T= , LRG_750t1:c.1093-50T= NP_109587.1:n.1093-50T=
XM_006722799.2:c.814-50T= XP_006722862.1:n.814-50T=
XM_011528133.1:c.523-50T= XP_011526435.1:n.523-50T=
NM_030662.4:c.1093-50T= MANE Select NP_109587.1:n.1093-50T=
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