Canonical Allele Identifier: CA2319219774
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090660C= , CM000681.2:g.4090660C= GRCh38
NC_000019.9:g.4090658C= , CM000681.1:g.4090658C= GRCh37
NC_000019.8:g.4041658C= NCBI36
NG_007996.1:g.38469G= , LRG_750:g.38469G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1580G=
ENST00000688002.1:n.3292G=
ENST00000688751.1:n.277G=
ENST00000689792.1:n.1045G=
ENST00000262948.10:c.1141G= MANE Select ENSP00000262948.4:p.Gly381=
ENST00000262948.9:c.1141G= ENSP00000262948.3:p.Gly381=
ENST00000394867.8:c.850G= ENSP00000378336.1:p.Gly284=
ENST00000597263.5:n.326G=
ENST00000599021.1:c.251G=
ENST00000600584.5:n.2590G=
ENST00000601786.5:n.1442G=
NM_030662.3:c.1141G= , LRG_750t1:c.1141G= NP_109587.1:p.Gly381=
XM_006722799.2:c.862G= XP_006722862.1:p.Gly288=
XM_011528133.1:c.571G= XP_011526435.1:p.Gly191=
NM_030662.4:c.1141G= MANE Select NP_109587.1:p.Gly381=