Canonical Allele Identifier: CA2319219872
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090857G= , CM000681.2:g.4090857G= GRCh38
NC_000019.9:g.4090855G= , CM000681.1:g.4090855G= GRCh37
NC_000019.8:g.4041855G= NCBI36
NG_007996.1:g.38272C= , LRG_750:g.38272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-149C=
ENST00000688002.1:n.3244-149C=
ENST00000688751.1:n.229-149C=
ENST00000689792.1:n.997-149C=
ENST00000262948.10:c.1093-149C= MANE Select ENSP00000262948.4:n.1093-149C=
ENST00000262948.9:c.1093-149C= ENSP00000262948.3:n.1093-149C=
ENST00000394867.8:c.802-149C= ENSP00000378336.1:n.802-149C=
ENST00000597263.5:n.278-149C=
ENST00000599021.1:c.203-149C=
ENST00000600584.5:n.2542-149C=
ENST00000601786.5:n.1394-149C=
NM_030662.3:c.1093-149C= , LRG_750t1:c.1093-149C= NP_109587.1:n.1093-149C=
XM_006722799.2:c.814-149C= XP_006722862.1:n.814-149C=
XM_011528133.1:c.523-149C= XP_011526435.1:n.523-149C=
NM_030662.4:c.1093-149C= MANE Select NP_109587.1:n.1093-149C=