Canonical Allele Identifier: CA1548139440
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1748231545

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882079del , CM000667.2:g.56882079del GRCh38
NC_000005.9:g.56177906del , CM000667.1:g.56177906del GRCh37
NC_000005.8:g.56213663del NCBI36
NG_031884.1:g.72007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2879del MANE Select ENSP00000382423.3:p.Gly960AlafsTer8
ENST00000399503.3:c.2879del ENSP00000382423.3:p.Gly960AlafsTer8
NM_005921.1:c.2879del NP_005912.1:p.Gly960AlafsTer8
XM_005248519.3:c.2501del XP_005248576.2:p.Gly834AlafsTer8
XM_011543406.1:c.2624del XP_011541708.1:p.Gly875AlafsTer8
XM_011543407.1:c.2600del XP_011541709.1:p.Gly867AlafsTer8
XM_011543408.1:c.2879del XP_011541710.1:p.Gly960AlafsTer8
XM_017009484.1:c.2468del XP_016864973.1:p.Gly823AlafsTer8
XM_017009485.1:c.2390del XP_016864974.1:p.Gly797AlafsTer8
XR_001742068.2:n.2910del
NM_005921.2:c.2879del MANE Select NP_005912.1:p.Gly960AlafsTer8