Canonical Allele Identifier: CA3273012
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs750114442
gnomAD v2: 5-56177561-G-A
gnomAD v3: 5-56881734-G-A
gnomAD v4: 5-56881734-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881734G>A , CM000667.2:g.56881734G>A GRCh38
NC_000005.9:g.56177561G>A , CM000667.1:g.56177561G>A GRCh37
NC_000005.8:g.56213318G>A NCBI36
NG_031884.1:g.71662G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2534G>A MANE Select ENSP00000382423.3:p.Ser845Asn
ENST00000399503.3:c.2534G>A ENSP00000382423.3:p.Ser845Asn
NM_005921.1:c.2534G>A NP_005912.1:p.Ser845Asn
XM_005248519.3:c.2156G>A XP_005248576.2:p.Ser719Asn
XM_011543406.1:c.2279G>A XP_011541708.1:p.Ser760Asn
XM_011543407.1:c.2255G>A XP_011541709.1:p.Ser752Asn
XM_011543408.1:c.2534G>A XP_011541710.1:p.Ser845Asn
XM_017009484.1:c.2123G>A XP_016864973.1:p.Ser708Asn
XM_017009485.1:c.2045G>A XP_016864974.1:p.Ser682Asn
XR_001742068.2:n.2565G>A
NM_005921.2:c.2534G>A MANE Select NP_005912.1:p.Ser845Asn