Canonical Allele Identifier: CA2319219720
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090581A= , CM000681.2:g.4090581A= GRCh38
NC_000019.9:g.4090579A= , CM000681.1:g.4090579A= GRCh37
NC_000019.8:g.4041579A= NCBI36
NG_007996.1:g.38548T= , LRG_750:g.38548T=

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.1659T=
ENST00000688002.1:n.3371T=
ENST00000688751.1:n.356T=
ENST00000689792.1:n.1124T=
ENST00000262948.10:c.*17T= MANE Select ENSP00000262948.4:n.*17T=
ENST00000262948.9:c.*17T= ENSP00000262948.3:n.*17T=
ENST00000394867.8:c.*17T= ENSP00000378336.1:n.*17T=
ENST00000597263.5:n.405T=
ENST00000600584.5:n.2669T=
ENST00000601786.5:n.1521T=
NM_030662.3:c.*17T= , LRG_750t1:c.*17T= NP_109587.1:n.*17T=
XM_006722799.2:c.*17T= XP_006722862.1:n.*17T=
XM_011528133.1:c.*17T= XP_011526435.1:n.*17T=
NM_030662.4:c.*17T= MANE Select NP_109587.1:n.*17T=