Canonical Allele Identifier: CA645563890
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875209_56875216del , CM000667.2:g.56875209_56875216del GRCh38
NC_000005.9:g.56171036_56171043del , CM000667.1:g.56171036_56171043del GRCh37
NC_000005.8:g.56206793_56206800del NCBI36
NG_031884.1:g.65137_65144del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1864_1871del MANE Select ENSP00000382423.3:p.Ser622AspfsTer21
ENST00000399503.3:c.1864_1871del ENSP00000382423.3:p.Ser622AspfsTer21
NM_005921.1:c.1864_1871del NP_005912.1:p.Ser622AspfsTer21
XM_005248519.3:c.1486_1493del XP_005248576.2:p.Ser496AspfsTer21
XM_011543406.1:c.1609_1616del XP_011541708.1:p.Ser537AspfsTer21
XM_011543407.1:c.1686+2204_1686+2211del XP_011541709.1:n.1686+2204_1686+2211del
XM_011543408.1:c.1864_1871del XP_011541710.1:p.Ser622AspfsTer21
XM_017009484.1:c.1453_1460del XP_016864973.1:p.Ser485AspfsTer21
XM_017009485.1:c.1375_1382del XP_016864974.1:p.Ser459AspfsTer21
XR_001742068.2:n.1895_1902del
NM_005921.2:c.1864_1871del MANE Select NP_005912.1:p.Ser622AspfsTer21