Canonical Allele Identifier: CA2319219554
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090329T= , CM000681.2:g.4090329T= GRCh38
NC_000019.9:g.4090327T= , CM000681.1:g.4090327T= GRCh37
NC_000019.8:g.4041327T= NCBI36
NG_007996.1:g.38800A= , LRG_750:g.38800A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1376A=
ENST00000262948.10:c.*269A= MANE Select ENSP00000262948.4:n.*269A=
ENST00000262948.9:c.*269A= ENSP00000262948.3:n.*269A=
ENST00000600584.5:n.2921A=
ENST00000601786.5:n.1773A=
NM_030662.3:c.*269A= , LRG_750t1:c.*269A= NP_109587.1:n.*269A=
XM_006722799.2:c.*269A= XP_006722862.1:n.*269A=
XM_011528133.1:c.*269A= XP_011526435.1:n.*269A=
NM_030662.4:c.*269A= MANE Select NP_109587.1:n.*269A=