Canonical Allele Identifier: CA2319219602
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090403C= , CM000681.2:g.4090403C= GRCh38
NC_000019.9:g.4090401C= , CM000681.1:g.4090401C= GRCh37
NC_000019.8:g.4041401C= NCBI36
NG_007996.1:g.38726G= , LRG_750:g.38726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1837G=
ENST00000688751.1:n.534G=
ENST00000689792.1:n.1302G=
ENST00000262948.10:c.*195G= MANE Select ENSP00000262948.4:n.*195G=
ENST00000262948.9:c.*195G= ENSP00000262948.3:n.*195G=
ENST00000394867.8:c.*195G= ENSP00000378336.1:n.*195G=
ENST00000600584.5:n.2847G=
ENST00000601786.5:n.1699G=
NM_030662.3:c.*195G= , LRG_750t1:c.*195G= NP_109587.1:n.*195G=
XM_006722799.2:c.*195G= XP_006722862.1:n.*195G=
XM_011528133.1:c.*195G= XP_011526435.1:n.*195G=
NM_030662.4:c.*195G= MANE Select NP_109587.1:n.*195G=