Canonical Allele Identifier: CA2319224421
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4099320A= , CM000681.2:g.4099320A= GRCh38
NC_000019.9:g.4099318A= , CM000681.1:g.4099318A= GRCh37
NC_000019.8:g.4050318A= NCBI36
NG_007996.1:g.29809T= , LRG_750:g.29809T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1239T=
ENST00000687128.1:n.1239T=
ENST00000688002.1:n.1094T=
ENST00000689792.1:n.704T=
ENST00000262948.10:c.800T= MANE Select ENSP00000262948.4:p.Ile267=
ENST00000262948.9:c.800T= ENSP00000262948.3:p.Ile267=
ENST00000394867.8:c.509T= ENSP00000378336.1:p.Ile170=
ENST00000593364.5:n.747T=
ENST00000595715.1:n.615T=
ENST00000597263.5:n.169+1699T=
ENST00000599021.1:c.29+1699T=
ENST00000600584.5:n.1360T=
ENST00000601786.5:n.1101T=
NM_030662.3:c.800T= , LRG_750t1:c.800T= NP_109587.1:p.Ile267=
XM_006722799.2:c.705+1699T= XP_006722862.1:n.705+1699T=
XM_011528133.1:c.230T= XP_011526435.1:p.Ile77=
XM_017026989.1:c.800T= XP_016882478.1:p.Ile267=
XM_017026990.1:c.705+1699T= XP_016882479.1:n.705+1699T=
NM_030662.4:c.800T= MANE Select NP_109587.1:p.Ile267=