Canonical Allele Identifier: CA2584876575
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090505-G-GC
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090505_4090506insC , CM000681.2:g.4090505_4090506insC GRCh38
NC_000019.9:g.4090503_4090504insC , CM000681.1:g.4090503_4090504insC GRCh37
NC_000019.8:g.4041503_4041504insC NCBI36
NG_007996.1:g.38623_38624insG , LRG_750:g.38623_38624insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1734_1735insG
ENST00000688002.1:n.3446_3447insG
ENST00000688751.1:n.431_432insG
ENST00000689792.1:n.1199_1200insG
ENST00000262948.10:c.*92_*93insG MANE Select ENSP00000262948.4:n.*92_*93insG
ENST00000262948.9:c.*92_*93insG ENSP00000262948.3:n.*92_*93insG
ENST00000394867.8:c.*92_*93insG ENSP00000378336.1:n.*92_*93insG
ENST00000597263.5:n.480_481insG
ENST00000600584.5:n.2744_2745insG
ENST00000601786.5:n.1596_1597insG
NM_030662.3:c.*92_*93insG , LRG_750t1:c.*92_*93insG NP_109587.1:n.*92_*93insG
XM_006722799.2:c.*92_*93insG XP_006722862.1:n.*92_*93insG
XM_011528133.1:c.*92_*93insG XP_011526435.1:n.*92_*93insG
NM_030662.4:c.*92_*93insG MANE Select NP_109587.1:n.*92_*93insG
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