Canonical Allele Identifier: CA3273034
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs778969592
gnomAD v2: 5-56177660-A-G
gnomAD v3: 5-56881833-A-G
gnomAD v4: 5-56881833-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881833A>G , CM000667.2:g.56881833A>G GRCh38
NC_000005.9:g.56177660A>G , CM000667.1:g.56177660A>G GRCh37
NC_000005.8:g.56213417A>G NCBI36
NG_031884.1:g.71761A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2633A>G MANE Select ENSP00000382423.3:p.Asp878Gly
ENST00000399503.3:c.2633A>G ENSP00000382423.3:p.Asp878Gly
NM_005921.1:c.2633A>G NP_005912.1:p.Asp878Gly
XM_005248519.3:c.2255A>G XP_005248576.2:p.Asp752Gly
XM_011543406.1:c.2378A>G XP_011541708.1:p.Asp793Gly
XM_011543407.1:c.2354A>G XP_011541709.1:p.Asp785Gly
XM_011543408.1:c.2633A>G XP_011541710.1:p.Asp878Gly
XM_017009484.1:c.2222A>G XP_016864973.1:p.Asp741Gly
XM_017009485.1:c.2144A>G XP_016864974.1:p.Asp715Gly
XR_001742068.2:n.2664A>G
NM_005921.2:c.2633A>G MANE Select NP_005912.1:p.Asp878Gly