Canonical Allele Identifier: CA304445589
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs914394236

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090426del , CM000681.2:g.4090426del GRCh38
NC_000019.9:g.4090424del , CM000681.1:g.4090424del GRCh37
NC_000019.8:g.4041424del NCBI36
NG_007996.1:g.38705del , LRG_750:g.38705del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1816del
ENST00000688751.1:n.513del
ENST00000689792.1:n.1281del
ENST00000262948.10:c.*174del MANE Select ENSP00000262948.4:n.*174del
ENST00000262948.9:c.*174del ENSP00000262948.3:n.*174del
ENST00000394867.8:c.*174del ENSP00000378336.1:n.*174del
ENST00000600584.5:n.2826del
ENST00000601786.5:n.1678del
NM_030662.3:c.*174del , LRG_750t1:c.*174del NP_109587.1:n.*174del
XM_006722799.2:c.*174del XP_006722862.1:n.*174del
XM_011528133.1:c.*174del XP_011526435.1:n.*174del
NM_030662.4:c.*174del MANE Select NP_109587.1:n.*174del