Canonical Allele Identifier: CA2319219833
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090782G= , CM000681.2:g.4090782G= GRCh38
NC_000019.9:g.4090780G= , CM000681.1:g.4090780G= GRCh37
NC_000019.8:g.4041780G= NCBI36
NG_007996.1:g.38347C= , LRG_750:g.38347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-74C=
ENST00000688002.1:n.3244-74C=
ENST00000688751.1:n.229-74C=
ENST00000689792.1:n.997-74C=
ENST00000262948.10:c.1093-74C= MANE Select ENSP00000262948.4:n.1093-74C=
ENST00000262948.9:c.1093-74C= ENSP00000262948.3:n.1093-74C=
ENST00000394867.8:c.802-74C= ENSP00000378336.1:n.802-74C=
ENST00000597263.5:n.278-74C=
ENST00000599021.1:c.203-74C=
ENST00000600584.5:n.2542-74C=
ENST00000601786.5:n.1394-74C=
NM_030662.3:c.1093-74C= , LRG_750t1:c.1093-74C= NP_109587.1:n.1093-74C=
XM_006722799.2:c.814-74C= XP_006722862.1:n.814-74C=
XM_011528133.1:c.523-74C= XP_011526435.1:n.523-74C=
NM_030662.4:c.1093-74C= MANE Select NP_109587.1:n.1093-74C=
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