Canonical Allele Identifier: CA2319219672
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090498A= , CM000681.2:g.4090498A= GRCh38
NC_000019.9:g.4090496A= , CM000681.1:g.4090496A= GRCh37
NC_000019.8:g.4041496A= NCBI36
NG_007996.1:g.38631T= , LRG_750:g.38631T=

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.1742T=
ENST00000688002.1:n.3454T=
ENST00000688751.1:n.439T=
ENST00000689792.1:n.1207T=
ENST00000262948.10:c.*100T= MANE Select ENSP00000262948.4:n.*100T=
ENST00000262948.9:c.*100T= ENSP00000262948.3:n.*100T=
ENST00000394867.8:c.*100T= ENSP00000378336.1:n.*100T=
ENST00000597263.5:n.488T=
ENST00000600584.5:n.2752T=
ENST00000601786.5:n.1604T=
NM_030662.3:c.*100T= , LRG_750t1:c.*100T= NP_109587.1:n.*100T=
XM_006722799.2:c.*100T= XP_006722862.1:n.*100T=
XM_011528133.1:c.*100T= XP_011526435.1:n.*100T=
NM_030662.4:c.*100T= MANE Select NP_109587.1:n.*100T=