Canonical Allele Identifier: CA2584876560
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090498_4090500del , CM000681.2:g.4090498_4090500del GRCh38
NC_000019.9:g.4090496_4090498del , CM000681.1:g.4090496_4090498del GRCh37
NC_000019.8:g.4041496_4041498del NCBI36
NG_007996.1:g.38632_38634del , LRG_750:g.38632_38634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1743_1745del
ENST00000688002.1:n.3455_3457del
ENST00000688751.1:n.440_442del
ENST00000689792.1:n.1208_1210del
ENST00000262948.10:c.*101_*103del MANE Select ENSP00000262948.4:n.*101_*103del
ENST00000262948.9:c.*101_*103del ENSP00000262948.3:n.*101_*103del
ENST00000394867.8:c.*101_*103del ENSP00000378336.1:n.*101_*103del
ENST00000597263.5:n.489_491del
ENST00000600584.5:n.2753_2755del
ENST00000601786.5:n.1605_1607del
NM_030662.3:c.*101_*103del , LRG_750t1:c.*101_*103del NP_109587.1:n.*101_*103del
XM_006722799.2:c.*101_*103del XP_006722862.1:n.*101_*103del
XM_011528133.1:c.*101_*103del XP_011526435.1:n.*101_*103del
NM_030662.4:c.*101_*103del MANE Select NP_109587.1:n.*101_*103del