Canonical Allele Identifier: CA2319219557
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2040842602

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090337del , CM000681.2:g.4090337del GRCh38
NC_000019.9:g.4090335del , CM000681.1:g.4090335del GRCh37
NC_000019.8:g.4041335del NCBI36
NG_007996.1:g.38794del , LRG_750:g.38794del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1370del
ENST00000262948.10:c.*263del MANE Select ENSP00000262948.4:n.*263del
ENST00000262948.9:c.*263del ENSP00000262948.3:n.*263del
ENST00000394867.8:c.*263del ENSP00000378336.1:n.*263del
ENST00000600584.5:n.2915del
ENST00000601786.5:n.1767del
NM_030662.3:c.*263del , LRG_750t1:c.*263del NP_109587.1:n.*263del
XM_006722799.2:c.*263del XP_006722862.1:n.*263del
XM_011528133.1:c.*263del XP_011526435.1:n.*263del
NM_030662.4:c.*263del MANE Select NP_109587.1:n.*263del