Canonical Allele Identifier: CA2319219755
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090627G= , CM000681.2:g.4090627G= GRCh38
NC_000019.9:g.4090625G= , CM000681.1:g.4090625G= GRCh37
NC_000019.8:g.4041625G= NCBI36
NG_007996.1:g.38502C= , LRG_750:g.38502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1613C=
ENST00000688002.1:n.3325C=
ENST00000688751.1:n.310C=
ENST00000689792.1:n.1078C=
ENST00000262948.10:c.1174C= MANE Select ENSP00000262948.4:p.Pro392=
ENST00000262948.9:c.1174C= ENSP00000262948.3:p.Pro392=
ENST00000394867.8:c.883C= ENSP00000378336.1:p.Pro295=
ENST00000597263.5:n.359C=
ENST00000599021.1:c.284C=
ENST00000600584.5:n.2623C=
ENST00000601786.5:n.1475C=
NM_030662.3:c.1174C= , LRG_750t1:c.1174C= NP_109587.1:p.Pro392=
XM_006722799.2:c.895C= XP_006722862.1:p.Pro299=
XM_011528133.1:c.604C= XP_011526435.1:p.Pro202=
NM_030662.4:c.1174C= MANE Select NP_109587.1:p.Pro392=