Canonical Allele Identifier: CA279890
Gene: MAP3K20 HGNC NCBI
MAP3K20-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218144
dbSNP Id: rs863225437

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.173232359T>G , CM000664.2:g.173232359T>G GRCh38
NC_000002.11:g.174097087T>G , CM000664.1:g.174097087T>G GRCh37
NC_000002.10:g.173805333T>G NCBI36
NG_029373.1:g.161523T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375213.8:c.1103T>G (MAP3K20) MANE Select ENSP00000364361.3:p.Phe368Cys
ENST00000375213.7:c.1103T>G (MAP3K20) ENSP00000364361.3:p.Phe368Cys
ENST00000409176.6:c.1103T>G (MAP3K20) ENSP00000387259.2:p.Phe368Cys
NM_016653.2:c.1103T>G (MAP3K20) NP_057737.2:p.Phe368Cys
NR_033882.1:n.464-16523A>C (MAP3K20-AS1)
XM_005246640.1:c.1103T>G (MAP3K20) XP_005246697.1:p.Phe368Cys
XM_005246640.2:c.1103T>G (MAP3K20) XP_005246697.1:p.Phe368Cys
NM_016653.3:c.1103T>G (MAP3K20) MANE Select NP_057737.2:p.Phe368Cys