Canonical Allele Identifier: CA2319219791
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090706G= , CM000681.2:g.4090706G= GRCh38
NC_000019.9:g.4090704G= , CM000681.1:g.4090704G= GRCh37
NC_000019.8:g.4041704G= NCBI36
NG_007996.1:g.38423C= , LRG_750:g.38423C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1534C=
ENST00000688002.1:n.3246C=
ENST00000688751.1:n.231C=
ENST00000689792.1:n.999C=
ENST00000262948.10:c.1095C= MANE Select ENSP00000262948.4:p.Asn365=
ENST00000262948.9:c.1095C= ENSP00000262948.3:p.Asn365=
ENST00000394867.8:c.804C= ENSP00000378336.1:p.Asn268=
ENST00000597263.5:n.280C=
ENST00000599021.1:c.205C=
ENST00000600584.5:n.2544C=
ENST00000601786.5:n.1396C=
NM_030662.3:c.1095C= , LRG_750t1:c.1095C= NP_109587.1:p.Asn365=
XM_006722799.2:c.816C= XP_006722862.1:p.Asn272=
XM_011528133.1:c.525C= XP_011526435.1:p.Asn175=
NM_030662.4:c.1095C= MANE Select NP_109587.1:p.Asn365=