Canonical Allele Identifier: CA2584876551
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090488_4090490del , CM000681.2:g.4090488_4090490del GRCh38
NC_000019.9:g.4090486_4090488del , CM000681.1:g.4090486_4090488del GRCh37
NC_000019.8:g.4041486_4041488del NCBI36
NG_007996.1:g.38640_38642del , LRG_750:g.38640_38642del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1751_1753del
ENST00000688002.1:n.3463_3465del
ENST00000688751.1:n.448_450del
ENST00000689792.1:n.1216_1218del
ENST00000262948.10:c.*109_*111del MANE Select ENSP00000262948.4:n.*109_*111del
ENST00000262948.9:c.*109_*111del ENSP00000262948.3:n.*109_*111del
ENST00000394867.8:c.*109_*111del ENSP00000378336.1:n.*109_*111del
ENST00000597263.5:n.497_499del
ENST00000600584.5:n.2761_2763del
ENST00000601786.5:n.1613_1615del
NM_030662.3:c.*109_*111del , LRG_750t1:c.*109_*111del NP_109587.1:n.*109_*111del
XM_006722799.2:c.*109_*111del XP_006722862.1:n.*109_*111del
XM_011528133.1:c.*109_*111del XP_011526435.1:n.*109_*111del
NM_030662.4:c.*109_*111del MANE Select NP_109587.1:n.*109_*111del