Canonical Allele Identifier: CA2319219708
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090561G= , CM000681.2:g.4090561G= GRCh38
NC_000019.9:g.4090559G= , CM000681.1:g.4090559G= GRCh37
NC_000019.8:g.4041559G= NCBI36
NG_007996.1:g.38568C= , LRG_750:g.38568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1679C=
ENST00000688002.1:n.3391C=
ENST00000688751.1:n.376C=
ENST00000689792.1:n.1144C=
ENST00000262948.10:c.*37C= MANE Select ENSP00000262948.4:n.*37C=
ENST00000262948.9:c.*37C= ENSP00000262948.3:n.*37C=
ENST00000394867.8:c.*37C= ENSP00000378336.1:n.*37C=
ENST00000597263.5:n.425C=
ENST00000600584.5:n.2689C=
ENST00000601786.5:n.1541C=
NM_030662.3:c.*37C= , LRG_750t1:c.*37C= NP_109587.1:n.*37C=
XM_006722799.2:c.*37C= XP_006722862.1:n.*37C=
XM_011528133.1:c.*37C= XP_011526435.1:n.*37C=
NM_030662.4:c.*37C= MANE Select NP_109587.1:n.*37C=