Canonical Allele Identifier: CA2673909469
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875435del , CM000667.2:g.56875435del GRCh38
NC_000005.9:g.56171262del , CM000667.1:g.56171262del GRCh37
NC_000005.8:g.56207019del NCBI36
NG_031884.1:g.65363del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1965+125del MANE Select ENSP00000382423.3:n.1965+125del
ENST00000399503.3:c.1965+125del ENSP00000382423.3:n.1965+125del
NM_005921.1:c.1965+125del NP_005912.1:n.1965+125del
XM_005248519.3:c.1587+125del XP_005248576.2:n.1587+125del
XM_011543406.1:c.1710+125del XP_011541708.1:n.1710+125del
XM_011543407.1:c.1686+2430del XP_011541709.1:n.1686+2430del
XM_011543408.1:c.1965+125del XP_011541710.1:n.1965+125del
XM_017009484.1:c.1554+125del XP_016864973.1:n.1554+125del
XM_017009485.1:c.1476+125del XP_016864974.1:n.1476+125del
XR_001742068.2:n.1996+125del
NM_005921.2:c.1965+125del MANE Select NP_005912.1:n.1965+125del