Canonical Allele Identifier: CA2319219757
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090631G= , CM000681.2:g.4090631G= GRCh38
NC_000019.9:g.4090629G= , CM000681.1:g.4090629G= GRCh37
NC_000019.8:g.4041629G= NCBI36
NG_007996.1:g.38498C= , LRG_750:g.38498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1609C=
ENST00000688002.1:n.3321C=
ENST00000688751.1:n.306C=
ENST00000689792.1:n.1074C=
ENST00000262948.10:c.1170C= MANE Select ENSP00000262948.4:p.Asn390=
ENST00000262948.9:c.1170C= ENSP00000262948.3:p.Asn390=
ENST00000394867.8:c.879C= ENSP00000378336.1:p.Asn293=
ENST00000597263.5:n.355C=
ENST00000599021.1:c.280C=
ENST00000600584.5:n.2619C=
ENST00000601786.5:n.1471C=
NM_030662.3:c.1170C= , LRG_750t1:c.1170C= NP_109587.1:p.Asn390=
XM_006722799.2:c.891C= XP_006722862.1:p.Asn297=
XM_011528133.1:c.600C= XP_011526435.1:p.Asn200=
NM_030662.4:c.1170C= MANE Select NP_109587.1:p.Asn390=