Canonical Allele Identifier: CA2584876397
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090330del , CM000681.2:g.4090330del GRCh38
NC_000019.9:g.4090328del , CM000681.1:g.4090328del GRCh37
NC_000019.8:g.4041328del NCBI36
NG_007996.1:g.38803del , LRG_750:g.38803del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1379del
ENST00000262948.10:c.*272del MANE Select ENSP00000262948.4:n.*272del
ENST00000262948.9:c.*272del ENSP00000262948.3:n.*272del
ENST00000600584.5:n.2924del
ENST00000601786.5:n.1776del
NM_030662.3:c.*272del , LRG_750t1:c.*272del NP_109587.1:n.*272del
XM_006722799.2:c.*272del XP_006722862.1:n.*272del
XM_011528133.1:c.*272del XP_011526435.1:n.*272del
NM_030662.4:c.*272del MANE Select NP_109587.1:n.*272del