Canonical Allele Identifier: CA2319219745
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090615T= , CM000681.2:g.4090615T= GRCh38
NC_000019.9:g.4090613T= , CM000681.1:g.4090613T= GRCh37
NC_000019.8:g.4041613T= NCBI36
NG_007996.1:g.38514A= , LRG_750:g.38514A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1625A=
ENST00000688002.1:n.3337A=
ENST00000688751.1:n.322A=
ENST00000689792.1:n.1090A=
ENST00000262948.10:c.1186A= MANE Select ENSP00000262948.4:p.Thr396=
ENST00000262948.9:c.1186A= ENSP00000262948.3:p.Thr396=
ENST00000394867.8:c.895A= ENSP00000378336.1:p.Thr299=
ENST00000597263.5:n.371A=
ENST00000599021.1:c.296A=
ENST00000600584.5:n.2635A=
ENST00000601786.5:n.1487A=
NM_030662.3:c.1186A= , LRG_750t1:c.1186A= NP_109587.1:p.Thr396=
XM_006722799.2:c.907A= XP_006722862.1:p.Thr303=
XM_011528133.1:c.616A= XP_011526435.1:p.Thr206=
NM_030662.4:c.1186A= MANE Select NP_109587.1:p.Thr396=