Canonical Allele Identifier: CA359780665
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875096T>C , CM000667.2:g.56875096T>C GRCh38
NC_000005.9:g.56170923T>C , CM000667.1:g.56170923T>C GRCh37
NC_000005.8:g.56206680T>C NCBI36
NG_031884.1:g.65024T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1751T>C MANE Select ENSP00000382423.3:p.Leu584Pro
ENST00000399503.3:c.1751T>C ENSP00000382423.3:p.Leu584Pro
NM_005921.1:c.1751T>C NP_005912.1:p.Leu584Pro
XM_005248519.3:c.1373T>C XP_005248576.2:p.Leu458Pro
XM_011543406.1:c.1496T>C XP_011541708.1:p.Leu499Pro
XM_011543407.1:c.1686+2091T>C XP_011541709.1:n.1686+2091T>C
XM_011543408.1:c.1751T>C XP_011541710.1:p.Leu584Pro
XM_017009484.1:c.1340T>C XP_016864973.1:p.Leu447Pro
XM_017009485.1:c.1262T>C XP_016864974.1:p.Leu421Pro
XR_001742068.2:n.1782T>C
NM_005921.2:c.1751T>C MANE Select NP_005912.1:p.Leu584Pro