Canonical Allele Identifier: CA2584876611
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090531-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090531_4090532insA , CM000681.2:g.4090531_4090532insA GRCh38
NC_000019.9:g.4090529_4090530insA , CM000681.1:g.4090529_4090530insA GRCh37
NC_000019.8:g.4041529_4041530insA NCBI36
NG_007996.1:g.38597_38598insT , LRG_750:g.38597_38598insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1708_1709insT
ENST00000688002.1:n.3420_3421insT
ENST00000688751.1:n.405_406insT
ENST00000689792.1:n.1173_1174insT
ENST00000262948.10:c.*66_*67insT MANE Select ENSP00000262948.4:n.*66_*67insT
ENST00000262948.9:c.*66_*67insT ENSP00000262948.3:n.*66_*67insT
ENST00000394867.8:c.*66_*67insT ENSP00000378336.1:n.*66_*67insT
ENST00000597263.5:n.454_455insT
ENST00000600584.5:n.2718_2719insT
ENST00000601786.5:n.1570_1571insT
NM_030662.3:c.*66_*67insT , LRG_750t1:c.*66_*67insT NP_109587.1:n.*66_*67insT
XM_006722799.2:c.*66_*67insT XP_006722862.1:n.*66_*67insT
XM_011528133.1:c.*66_*67insT XP_011526435.1:n.*66_*67insT
NM_030662.4:c.*66_*67insT MANE Select NP_109587.1:n.*66_*67insT
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