Canonical Allele Identifier: CA2584876773
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090834-T-TCC
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090837_4090838dup , CM000681.2:g.4090837_4090838dup GRCh38
NC_000019.9:g.4090835_4090836dup , CM000681.1:g.4090835_4090836dup GRCh37
NC_000019.8:g.4041835_4041836dup NCBI36
NG_007996.1:g.38293_38294dup , LRG_750:g.38293_38294dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-128_1532-127dup
ENST00000688002.1:n.3244-128_3244-127dup
ENST00000688751.1:n.229-128_229-127dup
ENST00000689792.1:n.997-128_997-127dup
ENST00000262948.10:c.1093-128_1093-127dup MANE Select ENSP00000262948.4:n.1093-128_1093-127dup
ENST00000262948.9:c.1093-128_1093-127dup ENSP00000262948.3:n.1093-128_1093-127dup
ENST00000394867.8:c.802-128_802-127dup ENSP00000378336.1:n.802-128_802-127dup
ENST00000597263.5:n.278-128_278-127dup
ENST00000599021.1:c.203-128_203-127dup
ENST00000600584.5:n.2542-128_2542-127dup
ENST00000601786.5:n.1394-128_1394-127dup
NM_030662.3:c.1093-128_1093-127dup , LRG_750t1:c.1093-128_1093-127dup NP_109587.1:n.1093-128_1093-127dup
XM_006722799.2:c.814-128_814-127dup XP_006722862.1:n.814-128_814-127dup
XM_011528133.1:c.523-128_523-127dup XP_011526435.1:n.523-128_523-127dup
NM_030662.4:c.1093-128_1093-127dup MANE Select NP_109587.1:n.1093-128_1093-127dup
Search 100 bp 5'
Search 100 bp 3'