Canonical Allele Identifier: CA2319219659
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090474T= , CM000681.2:g.4090474T= GRCh38
NC_000019.9:g.4090472T= , CM000681.1:g.4090472T= GRCh37
NC_000019.8:g.4041472T= NCBI36
NG_007996.1:g.38655A= , LRG_750:g.38655A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1766A=
ENST00000688002.1:n.3478A=
ENST00000688751.1:n.463A=
ENST00000689792.1:n.1231A=
ENST00000262948.10:c.*124A= MANE Select ENSP00000262948.4:n.*124A=
ENST00000262948.9:c.*124A= ENSP00000262948.3:n.*124A=
ENST00000394867.8:c.*124A= ENSP00000378336.1:n.*124A=
ENST00000597263.5:n.512A=
ENST00000600584.5:n.2776A=
ENST00000601786.5:n.1628A=
NM_030662.3:c.*124A= , LRG_750t1:c.*124A= NP_109587.1:n.*124A=
XM_006722799.2:c.*124A= XP_006722862.1:n.*124A=
XM_011528133.1:c.*124A= XP_011526435.1:n.*124A=
NM_030662.4:c.*124A= MANE Select NP_109587.1:n.*124A=