Canonical Allele Identifier: CA645563889
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875112_56875119dup , CM000667.2:g.56875112_56875119dup GRCh38
NC_000005.9:g.56170939_56170946dup , CM000667.1:g.56170939_56170946dup GRCh37
NC_000005.8:g.56206696_56206703dup NCBI36
NG_031884.1:g.65040_65047dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1767_1774dup MANE Select ENSP00000382423.3:p.Ser592MetfsTer?
ENST00000399503.3:c.1767_1774dup ENSP00000382423.3:p.Ser592MetfsTer?
NM_005921.1:c.1767_1774dup NP_005912.1:p.Ser592MetfsTer?
XM_005248519.3:c.1389_1396dup XP_005248576.2:p.Ser466MetfsTer?
XM_011543406.1:c.1512_1519dup XP_011541708.1:p.Ser507MetfsTer?
XM_011543407.1:c.1686+2107_1686+2114dup XP_011541709.1:n.1686+2107_1686+2114dup
XM_011543408.1:c.1767_1774dup XP_011541710.1:p.Ser592MetfsTer?
XM_017009484.1:c.1356_1363dup XP_016864973.1:p.Ser455MetfsTer?
XM_017009485.1:c.1278_1285dup XP_016864974.1:p.Ser429MetfsTer?
XR_001742068.2:n.1798_1805dup
NM_005921.2:c.1767_1774dup MANE Select NP_005912.1:p.Ser592MetfsTer?