Canonical Allele Identifier: CA2319219558
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090335C= , CM000681.2:g.4090335C= GRCh38
NC_000019.9:g.4090333C= , CM000681.1:g.4090333C= GRCh37
NC_000019.8:g.4041333C= NCBI36
NG_007996.1:g.38794G= , LRG_750:g.38794G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1370G=
ENST00000262948.10:c.*263G= MANE Select ENSP00000262948.4:n.*263G=
ENST00000262948.9:c.*263G= ENSP00000262948.3:n.*263G=
ENST00000394867.8:c.*263G= ENSP00000378336.1:n.*263G=
ENST00000600584.5:n.2915G=
ENST00000601786.5:n.1767G=
NM_030662.3:c.*263G= , LRG_750t1:c.*263G= NP_109587.1:n.*263G=
XM_006722799.2:c.*263G= XP_006722862.1:n.*263G=
XM_011528133.1:c.*263G= XP_011526435.1:n.*263G=
NM_030662.4:c.*263G= MANE Select NP_109587.1:n.*263G=