Canonical Allele Identifier: CA2319221630
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094372C= , CM000681.2:g.4094372C= GRCh38
NC_000019.9:g.4094370C= , CM000681.1:g.4094370C= GRCh37
NC_000019.8:g.4045370C= NCBI36
NG_007996.1:g.34757G= , LRG_750:g.34757G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1531+81G=
ENST00000688002.1:n.3243+81G=
ENST00000688751.1:n.228+81G=
ENST00000689792.1:n.996+81G=
ENST00000262948.10:c.1092+81G= MANE Select ENSP00000262948.4:n.1092+81G=
ENST00000262948.9:c.1092+81G= ENSP00000262948.3:n.1092+81G=
ENST00000394867.8:c.801+81G= ENSP00000378336.1:n.801+81G=
ENST00000597263.5:n.277+81G=
ENST00000599021.1:c.202+81G=
ENST00000600584.5:n.2541+81G=
ENST00000601786.5:n.1393+81G=
NM_030662.3:c.1092+81G= , LRG_750t1:c.1092+81G= NP_109587.1:n.1092+81G=
XM_006722799.2:c.813+81G= XP_006722862.1:n.813+81G=
XM_011528133.1:c.522+81G= XP_011526435.1:n.522+81G=
NM_030662.4:c.1092+81G= MANE Select NP_109587.1:n.1092+81G=