Canonical Allele Identifier: CA2673908355
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859676del , CM000667.2:g.56859676del GRCh38
NC_000005.9:g.56155503del , CM000667.1:g.56155503del GRCh37
NC_000005.8:g.56191260del NCBI36
NG_031884.1:g.49604del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.634-39del MANE Select ENSP00000382423.3:n.634-39del
ENST00000399503.3:c.634-39del ENSP00000382423.3:n.634-39del
NM_005921.1:c.634-39del NP_005912.1:n.634-39del
XM_005248519.3:c.256-39del XP_005248576.2:n.256-39del
XM_011543406.1:c.379-39del XP_011541708.1:n.379-39del
XM_011543407.1:c.634-39del XP_011541709.1:n.634-39del
XM_011543408.1:c.634-39del XP_011541710.1:n.634-39del
XM_017009484.1:c.223-39del XP_016864973.1:n.223-39del
XM_017009485.1:c.145-39del XP_016864974.1:n.145-39del
XR_001742068.2:n.665-39del
NM_005921.2:c.634-39del MANE Select NP_005912.1:n.634-39del