Canonical Allele Identifier: CA882241164
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1477673517

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090403del , CM000681.2:g.4090403del GRCh38
NC_000019.9:g.4090401del , CM000681.1:g.4090401del GRCh37
NC_000019.8:g.4041401del NCBI36
NG_007996.1:g.38729del , LRG_750:g.38729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1840del
ENST00000688751.1:n.537del
ENST00000689792.1:n.1305del
ENST00000262948.10:c.*198del MANE Select ENSP00000262948.4:n.*198del
ENST00000262948.9:c.*198del ENSP00000262948.3:n.*198del
ENST00000394867.8:c.*198del ENSP00000378336.1:n.*198del
ENST00000600584.5:n.2850del
ENST00000601786.5:n.1702del
NM_030662.3:c.*198del , LRG_750t1:c.*198del NP_109587.1:n.*198del
XM_006722799.2:c.*198del XP_006722862.1:n.*198del
XM_011528133.1:c.*198del XP_011526435.1:n.*198del
NM_030662.4:c.*198del MANE Select NP_109587.1:n.*198del