Canonical Allele Identifier: CA2319219712
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090572G= , CM000681.2:g.4090572G= GRCh38
NC_000019.9:g.4090570G= , CM000681.1:g.4090570G= GRCh37
NC_000019.8:g.4041570G= NCBI36
NG_007996.1:g.38557C= , LRG_750:g.38557C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1668C=
ENST00000688002.1:n.3380C=
ENST00000688751.1:n.365C=
ENST00000689792.1:n.1133C=
ENST00000262948.10:c.*26C= MANE Select ENSP00000262948.4:n.*26C=
ENST00000262948.9:c.*26C= ENSP00000262948.3:n.*26C=
ENST00000394867.8:c.*26C= ENSP00000378336.1:n.*26C=
ENST00000597263.5:n.414C=
ENST00000600584.5:n.2678C=
ENST00000601786.5:n.1530C=
NM_030662.3:c.*26C= , LRG_750t1:c.*26C= NP_109587.1:n.*26C=
XM_006722799.2:c.*26C= XP_006722862.1:n.*26C=
XM_011528133.1:c.*26C= XP_011526435.1:n.*26C=
NM_030662.4:c.*26C= MANE Select NP_109587.1:n.*26C=