Canonical Allele Identifier: CA2584876584
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090512-C-CAGGA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090512_4090513insAGGA , CM000681.2:g.4090512_4090513insAGGA GRCh38
NC_000019.9:g.4090510_4090511insAGGA , CM000681.1:g.4090510_4090511insAGGA GRCh37
NC_000019.8:g.4041510_4041511insAGGA NCBI36
NG_007996.1:g.38616_38617insTCCT , LRG_750:g.38616_38617insTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1727_1728insTCCT
ENST00000688002.1:n.3439_3440insTCCT
ENST00000688751.1:n.424_425insTCCT
ENST00000689792.1:n.1192_1193insTCCT
ENST00000262948.10:c.*85_*86insTCCT MANE Select ENSP00000262948.4:n.*85_*86insTCCT
ENST00000262948.9:c.*85_*86insTCCT ENSP00000262948.3:n.*85_*86insTCCT
ENST00000394867.8:c.*85_*86insTCCT ENSP00000378336.1:n.*85_*86insTCCT
ENST00000597263.5:n.473_474insTCCT
ENST00000600584.5:n.2737_2738insTCCT
ENST00000601786.5:n.1589_1590insTCCT
NM_030662.3:c.*85_*86insTCCT , LRG_750t1:c.*85_*86insTCCT NP_109587.1:n.*85_*86insTCCT
XM_006722799.2:c.*85_*86insTCCT XP_006722862.1:n.*85_*86insTCCT
XM_011528133.1:c.*85_*86insTCCT XP_011526435.1:n.*85_*86insTCCT
NM_030662.4:c.*85_*86insTCCT MANE Select NP_109587.1:n.*85_*86insTCCT
Search 100 bp 5'
Search 100 bp 3'