Canonical Allele Identifier: CA645557016
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882016_56882057del , CM000667.2:g.56882016_56882057del GRCh38
NC_000005.9:g.56177843_56177884del , CM000667.1:g.56177843_56177884del GRCh37
NC_000005.8:g.56213600_56213641del NCBI36
NG_031884.1:g.71944_71985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2816_2857del MANE Select ENSP00000382423.3:p.Ser939Ter
ENST00000399503.3:c.2816_2857del ENSP00000382423.3:p.Ser939Ter
NM_005921.1:c.2816_2857del NP_005912.1:p.Ser939Ter
XM_005248519.3:c.2438_2479del XP_005248576.2:p.Ser813Ter
XM_011543406.1:c.2561_2602del XP_011541708.1:p.Ser854Ter
XM_011543407.1:c.2537_2578del XP_011541709.1:p.Ser846Ter
XM_011543408.1:c.2816_2857del XP_011541710.1:p.Ser939Ter
XM_017009484.1:c.2405_2446del XP_016864973.1:p.Ser802Ter
XM_017009485.1:c.2327_2368del XP_016864974.1:p.Ser776Ter
XR_001742068.2:n.2847_2888del
NM_005921.2:c.2816_2857del MANE Select NP_005912.1:p.Ser939Ter