Canonical Allele Identifier: CA359786269
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1261849638

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881856C>A , CM000667.2:g.56881856C>A GRCh38
NC_000005.9:g.56177683C>A , CM000667.1:g.56177683C>A GRCh37
NC_000005.8:g.56213440C>A NCBI36
NG_031884.1:g.71784C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2656C>A MANE Select ENSP00000382423.3:p.Gln886Lys
ENST00000399503.3:c.2656C>A ENSP00000382423.3:p.Gln886Lys
NM_005921.1:c.2656C>A NP_005912.1:p.Gln886Lys
XM_005248519.3:c.2278C>A XP_005248576.2:p.Gln760Lys
XM_011543406.1:c.2401C>A XP_011541708.1:p.Gln801Lys
XM_011543407.1:c.2377C>A XP_011541709.1:p.Gln793Lys
XM_011543408.1:c.2656C>A XP_011541710.1:p.Gln886Lys
XM_017009484.1:c.2245C>A XP_016864973.1:p.Gln749Lys
XM_017009485.1:c.2167C>A XP_016864974.1:p.Gln723Lys
XR_001742068.2:n.2687C>A
NM_005921.2:c.2656C>A MANE Select NP_005912.1:p.Gln886Lys