Canonical Allele Identifier: CA2319219704
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090556G= , CM000681.2:g.4090556G= GRCh38
NC_000019.9:g.4090554G= , CM000681.1:g.4090554G= GRCh37
NC_000019.8:g.4041554G= NCBI36
NG_007996.1:g.38573C= , LRG_750:g.38573C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1684C=
ENST00000688002.1:n.3396C=
ENST00000688751.1:n.381C=
ENST00000689792.1:n.1149C=
ENST00000262948.10:c.*42C= MANE Select ENSP00000262948.4:n.*42C=
ENST00000262948.9:c.*42C= ENSP00000262948.3:n.*42C=
ENST00000394867.8:c.*42C= ENSP00000378336.1:n.*42C=
ENST00000597263.5:n.430C=
ENST00000600584.5:n.2694C=
ENST00000601786.5:n.1546C=
NM_030662.3:c.*42C= , LRG_750t1:c.*42C= NP_109587.1:n.*42C=
XM_006722799.2:c.*42C= XP_006722862.1:n.*42C=
XM_011528133.1:c.*42C= XP_011526435.1:n.*42C=
NM_030662.4:c.*42C= MANE Select NP_109587.1:n.*42C=