Canonical Allele Identifier: CA359780669
Gene: MAP3K1 HGNC NCBI

Linked Data

gnomAD v4: 5-56875099-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875099G>A , CM000667.2:g.56875099G>A GRCh38
NC_000005.9:g.56170926G>A , CM000667.1:g.56170926G>A GRCh37
NC_000005.8:g.56206683G>A NCBI36
NG_031884.1:g.65027G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1754G>A MANE Select ENSP00000382423.3:p.Arg585Lys
ENST00000399503.3:c.1754G>A ENSP00000382423.3:p.Arg585Lys
NM_005921.1:c.1754G>A NP_005912.1:p.Arg585Lys
XM_005248519.3:c.1376G>A XP_005248576.2:p.Arg459Lys
XM_011543406.1:c.1499G>A XP_011541708.1:p.Arg500Lys
XM_011543407.1:c.1686+2094G>A XP_011541709.1:n.1686+2094G>A
XM_011543408.1:c.1754G>A XP_011541710.1:p.Arg585Lys
XM_017009484.1:c.1343G>A XP_016864973.1:p.Arg448Lys
XM_017009485.1:c.1265G>A XP_016864974.1:p.Arg422Lys
XR_001742068.2:n.1785G>A
NM_005921.2:c.1754G>A MANE Select NP_005912.1:p.Arg585Lys