Canonical Allele Identifier: CA1548128141
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1747376257

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857486_56857487del , CM000667.2:g.56857486_56857487del GRCh38
NC_000005.9:g.56153313_56153314del , CM000667.1:g.56153313_56153314del GRCh37
NC_000005.8:g.56189070_56189071del NCBI36
NG_031884.1:g.47414_47415del

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.633+736_633+737del MANE Select ENSP00000382423.3:n.633+736_633+737del
ENST00000399503.3:c.633+736_633+737del ENSP00000382423.3:n.633+736_633+737del
NM_005921.1:c.633+736_633+737del NP_005912.1:n.633+736_633+737del
XM_005248519.3:c.255+736_255+737del XP_005248576.2:n.255+736_255+737del
XM_011543406.1:c.378+736_378+737del XP_011541708.1:n.378+736_378+737del
XM_011543407.1:c.633+736_633+737del XP_011541709.1:n.633+736_633+737del
XM_011543408.1:c.633+736_633+737del XP_011541710.1:n.633+736_633+737del
XM_017009484.1:c.222+736_222+737del XP_016864973.1:n.222+736_222+737del
XM_017009485.1:c.144+736_144+737del XP_016864974.1:n.144+736_144+737del
XR_001742068.2:n.664+736_664+737del
NM_005921.2:c.633+736_633+737del MANE Select NP_005912.1:n.633+736_633+737del