Canonical Allele Identifier: CA2813356124
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090735_4090736insA , CM000681.2:g.4090735_4090736insA GRCh38
NC_000019.9:g.4090733_4090734insA , CM000681.1:g.4090733_4090734insA GRCh37
NC_000019.8:g.4041733_4041734insA NCBI36
NG_007996.1:g.38393_38394insT , LRG_750:g.38393_38394insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-28_1532-27insT
ENST00000688002.1:n.3244-28_3244-27insT
ENST00000688751.1:n.229-28_229-27insT
ENST00000689792.1:n.997-28_997-27insT
ENST00000262948.10:c.1093-28_1093-27insT MANE Select ENSP00000262948.4:n.1093-28_1093-27insT
ENST00000262948.9:c.1093-28_1093-27insT ENSP00000262948.3:n.1093-28_1093-27insT
ENST00000394867.8:c.802-28_802-27insT ENSP00000378336.1:n.802-28_802-27insT
ENST00000597263.5:n.278-28_278-27insT
ENST00000599021.1:c.203-28_203-27insT
ENST00000600584.5:n.2542-28_2542-27insT
ENST00000601786.5:n.1394-28_1394-27insT
NM_030662.3:c.1093-28_1093-27insT , LRG_750t1:c.1093-28_1093-27insT NP_109587.1:n.1093-28_1093-27insT
XM_006722799.2:c.814-28_814-27insT XP_006722862.1:n.814-28_814-27insT
XM_011528133.1:c.523-28_523-27insT XP_011526435.1:n.523-28_523-27insT
NM_030662.4:c.1093-28_1093-27insT MANE Select NP_109587.1:n.1093-28_1093-27insT
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