Canonical Allele Identifier: CA2584876795
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090859-TAGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090862_4090864del , CM000681.2:g.4090862_4090864del GRCh38
NC_000019.9:g.4090860_4090862del , CM000681.1:g.4090860_4090862del GRCh37
NC_000019.8:g.4041860_4041862del NCBI36
NG_007996.1:g.38267_38269del , LRG_750:g.38267_38269del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-154_1532-152del
ENST00000688002.1:n.3244-154_3244-152del
ENST00000688751.1:n.229-154_229-152del
ENST00000689792.1:n.997-154_997-152del
ENST00000262948.10:c.1093-154_1093-152del MANE Select ENSP00000262948.4:n.1093-154_1093-152del
ENST00000262948.9:c.1093-154_1093-152del ENSP00000262948.3:n.1093-154_1093-152del
ENST00000394867.8:c.802-154_802-152del ENSP00000378336.1:n.802-154_802-152del
ENST00000597263.5:n.278-154_278-152del
ENST00000599021.1:c.203-154_203-152del
ENST00000600584.5:n.2542-154_2542-152del
ENST00000601786.5:n.1394-154_1394-152del
NM_030662.3:c.1093-154_1093-152del , LRG_750t1:c.1093-154_1093-152del NP_109587.1:n.1093-154_1093-152del
XM_006722799.2:c.814-154_814-152del XP_006722862.1:n.814-154_814-152del
XM_011528133.1:c.523-154_523-152del XP_011526435.1:n.523-154_523-152del
NM_030662.4:c.1093-154_1093-152del MANE Select NP_109587.1:n.1093-154_1093-152del
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