Canonical Allele Identifier: CA2319219836
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090786T= , CM000681.2:g.4090786T= GRCh38
NC_000019.9:g.4090784T= , CM000681.1:g.4090784T= GRCh37
NC_000019.8:g.4041784T= NCBI36
NG_007996.1:g.38343A= , LRG_750:g.38343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-78A=
ENST00000688002.1:n.3244-78A=
ENST00000688751.1:n.229-78A=
ENST00000689792.1:n.997-78A=
ENST00000262948.10:c.1093-78A= MANE Select ENSP00000262948.4:n.1093-78A=
ENST00000262948.9:c.1093-78A= ENSP00000262948.3:n.1093-78A=
ENST00000394867.8:c.802-78A= ENSP00000378336.1:n.802-78A=
ENST00000597263.5:n.278-78A=
ENST00000599021.1:c.203-78A=
ENST00000600584.5:n.2542-78A=
ENST00000601786.5:n.1394-78A=
NM_030662.3:c.1093-78A= , LRG_750t1:c.1093-78A= NP_109587.1:n.1093-78A=
XM_006722799.2:c.814-78A= XP_006722862.1:n.814-78A=
XM_011528133.1:c.523-78A= XP_011526435.1:n.523-78A=
NM_030662.4:c.1093-78A= MANE Select NP_109587.1:n.1093-78A=
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