Canonical Allele Identifier: CA2673909957
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881533del , CM000667.2:g.56881533del GRCh38
NC_000005.9:g.56177360del , CM000667.1:g.56177360del GRCh37
NC_000005.8:g.56213117del NCBI36
NG_031884.1:g.71461del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2370-37del MANE Select ENSP00000382423.3:n.2370-37del
ENST00000399503.3:c.2370-37del ENSP00000382423.3:n.2370-37del
NM_005921.1:c.2370-37del NP_005912.1:n.2370-37del
XM_005248519.3:c.1992-37del XP_005248576.2:n.1992-37del
XM_011543406.1:c.2115-37del XP_011541708.1:n.2115-37del
XM_011543407.1:c.2091-37del XP_011541709.1:n.2091-37del
XM_011543408.1:c.2370-37del XP_011541710.1:n.2370-37del
XM_017009484.1:c.1959-37del XP_016864973.1:n.1959-37del
XM_017009485.1:c.1881-37del XP_016864974.1:n.1881-37del
XR_001742068.2:n.2401-37del
NM_005921.2:c.2370-37del MANE Select NP_005912.1:n.2370-37del