Canonical Allele Identifier: CA2584876759
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090817-CAG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090820_4090821del , CM000681.2:g.4090820_4090821del GRCh38
NC_000019.9:g.4090818_4090819del , CM000681.1:g.4090818_4090819del GRCh37
NC_000019.8:g.4041818_4041819del NCBI36
NG_007996.1:g.38310_38311del , LRG_750:g.38310_38311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-111_1532-110del
ENST00000688002.1:n.3244-111_3244-110del
ENST00000688751.1:n.229-111_229-110del
ENST00000689792.1:n.997-111_997-110del
ENST00000262948.10:c.1093-111_1093-110del MANE Select ENSP00000262948.4:n.1093-111_1093-110del
ENST00000262948.9:c.1093-111_1093-110del ENSP00000262948.3:n.1093-111_1093-110del
ENST00000394867.8:c.802-111_802-110del ENSP00000378336.1:n.802-111_802-110del
ENST00000597263.5:n.278-111_278-110del
ENST00000599021.1:c.203-111_203-110del
ENST00000600584.5:n.2542-111_2542-110del
ENST00000601786.5:n.1394-111_1394-110del
NM_030662.3:c.1093-111_1093-110del , LRG_750t1:c.1093-111_1093-110del NP_109587.1:n.1093-111_1093-110del
XM_006722799.2:c.814-111_814-110del XP_006722862.1:n.814-111_814-110del
XM_011528133.1:c.523-111_523-110del XP_011526435.1:n.523-111_523-110del
NM_030662.4:c.1093-111_1093-110del MANE Select NP_109587.1:n.1093-111_1093-110del
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