Canonical Allele Identifier: CA2673909914
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881423del , CM000667.2:g.56881423del GRCh38
NC_000005.9:g.56177250del , CM000667.1:g.56177250del GRCh37
NC_000005.8:g.56213007del NCBI36
NG_031884.1:g.71351del

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2370-147del MANE Select ENSP00000382423.3:n.2370-147del
ENST00000399503.3:c.2370-147del ENSP00000382423.3:n.2370-147del
NM_005921.1:c.2370-147del NP_005912.1:n.2370-147del
XM_005248519.3:c.1992-147del XP_005248576.2:n.1992-147del
XM_011543406.1:c.2115-147del XP_011541708.1:n.2115-147del
XM_011543407.1:c.2091-147del XP_011541709.1:n.2091-147del
XM_011543408.1:c.2370-147del XP_011541710.1:n.2370-147del
XM_017009484.1:c.1959-147del XP_016864973.1:n.1959-147del
XM_017009485.1:c.1881-147del XP_016864974.1:n.1881-147del
XR_001742068.2:n.2401-147del
NM_005921.2:c.2370-147del MANE Select NP_005912.1:n.2370-147del