Canonical Allele Identifier: CA2319219752
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090623C= , CM000681.2:g.4090623C= GRCh38
NC_000019.9:g.4090621C= , CM000681.1:g.4090621C= GRCh37
NC_000019.8:g.4041621C= NCBI36
NG_007996.1:g.38506G= , LRG_750:g.38506G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1617G=
ENST00000688002.1:n.3329G=
ENST00000688751.1:n.314G=
ENST00000689792.1:n.1082G=
ENST00000262948.10:c.1178G= MANE Select ENSP00000262948.4:p.Gly393=
ENST00000262948.9:c.1178G= ENSP00000262948.3:p.Gly393=
ENST00000394867.8:c.887G= ENSP00000378336.1:p.Gly296=
ENST00000597263.5:n.363G=
ENST00000599021.1:c.288G=
ENST00000600584.5:n.2627G=
ENST00000601786.5:n.1479G=
NM_030662.3:c.1178G= , LRG_750t1:c.1178G= NP_109587.1:p.Gly393=
XM_006722799.2:c.899G= XP_006722862.1:p.Gly300=
XM_011528133.1:c.608G= XP_011526435.1:p.Gly203=
NM_030662.4:c.1178G= MANE Select NP_109587.1:p.Gly393=