Canonical Allele Identifier: CA2319219732
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090596T= , CM000681.2:g.4090596T= GRCh38
NC_000019.9:g.4090594T= , CM000681.1:g.4090594T= GRCh37
NC_000019.8:g.4041594T= NCBI36
NG_007996.1:g.38533A= , LRG_750:g.38533A=

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.1644A=
ENST00000688002.1:n.3356A=
ENST00000688751.1:n.341A=
ENST00000689792.1:n.1109A=
ENST00000262948.10:c.*2A= MANE Select ENSP00000262948.4:n.*2A=
ENST00000262948.9:c.*2A= ENSP00000262948.3:n.*2A=
ENST00000394867.8:c.*2A= ENSP00000378336.1:n.*2A=
ENST00000597263.5:n.390A=
ENST00000600584.5:n.2654A=
ENST00000601786.5:n.1506A=
NM_030662.3:c.*2A= , LRG_750t1:c.*2A= NP_109587.1:n.*2A=
XM_006722799.2:c.*2A= XP_006722862.1:n.*2A=
XM_011528133.1:c.*2A= XP_011526435.1:n.*2A=
NM_030662.4:c.*2A= MANE Select NP_109587.1:n.*2A=