Canonical Allele Identifier: CA2319219597
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090398G= , CM000681.2:g.4090398G= GRCh38
NC_000019.9:g.4090396G= , CM000681.1:g.4090396G= GRCh37
NC_000019.8:g.4041396G= NCBI36
NG_007996.1:g.38731C= , LRG_750:g.38731C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1842C=
ENST00000688751.1:n.539C=
ENST00000689792.1:n.1307C=
ENST00000262948.10:c.*200C= MANE Select ENSP00000262948.4:n.*200C=
ENST00000262948.9:c.*200C= ENSP00000262948.3:n.*200C=
ENST00000394867.8:c.*200C= ENSP00000378336.1:n.*200C=
ENST00000600584.5:n.2852C=
ENST00000601786.5:n.1704C=
NM_030662.3:c.*200C= , LRG_750t1:c.*200C= NP_109587.1:n.*200C=
XM_006722799.2:c.*200C= XP_006722862.1:n.*200C=
XM_011528133.1:c.*200C= XP_011526435.1:n.*200C=
NM_030662.4:c.*200C= MANE Select NP_109587.1:n.*200C=