Canonical Allele Identifier: CA2319219879
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090868G= , CM000681.2:g.4090868G= GRCh38
NC_000019.9:g.4090866G= , CM000681.1:g.4090866G= GRCh37
NC_000019.8:g.4041866G= NCBI36
NG_007996.1:g.38261C= , LRG_750:g.38261C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-160C=
ENST00000688002.1:n.3244-160C=
ENST00000688751.1:n.229-160C=
ENST00000689792.1:n.997-160C=
ENST00000262948.10:c.1093-160C= MANE Select ENSP00000262948.4:n.1093-160C=
ENST00000262948.9:c.1093-160C= ENSP00000262948.3:n.1093-160C=
ENST00000394867.8:c.802-160C= ENSP00000378336.1:n.802-160C=
ENST00000597263.5:n.278-160C=
ENST00000599021.1:c.203-160C=
ENST00000600584.5:n.2542-160C=
ENST00000601786.5:n.1394-160C=
NM_030662.3:c.1093-160C= , LRG_750t1:c.1093-160C= NP_109587.1:n.1093-160C=
XM_006722799.2:c.814-160C= XP_006722862.1:n.814-160C=
XM_011528133.1:c.523-160C= XP_011526435.1:n.523-160C=
NM_030662.4:c.1093-160C= MANE Select NP_109587.1:n.1093-160C=