Canonical Allele Identifier: CA2584876606
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090529_4090530del , CM000681.2:g.4090529_4090530del GRCh38
NC_000019.9:g.4090527_4090528del , CM000681.1:g.4090527_4090528del GRCh37
NC_000019.8:g.4041527_4041528del NCBI36
NG_007996.1:g.38599_38600del , LRG_750:g.38599_38600del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1710_1711del
ENST00000688002.1:n.3422_3423del
ENST00000688751.1:n.407_408del
ENST00000689792.1:n.1175_1176del
ENST00000262948.10:c.*68_*69del MANE Select ENSP00000262948.4:n.*68_*69del
ENST00000262948.9:c.*68_*69del ENSP00000262948.3:n.*68_*69del
ENST00000394867.8:c.*68_*69del ENSP00000378336.1:n.*68_*69del
ENST00000597263.5:n.456_457del
ENST00000600584.5:n.2720_2721del
ENST00000601786.5:n.1572_1573del
NM_030662.3:c.*68_*69del , LRG_750t1:c.*68_*69del NP_109587.1:n.*68_*69del
XM_006722799.2:c.*68_*69del XP_006722862.1:n.*68_*69del
XM_011528133.1:c.*68_*69del XP_011526435.1:n.*68_*69del
NM_030662.4:c.*68_*69del MANE Select NP_109587.1:n.*68_*69del