Canonical Allele Identifier: CA359779215
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56872877C>G , CM000667.2:g.56872877C>G GRCh38
NC_000005.9:g.56168704C>G , CM000667.1:g.56168704C>G GRCh37
NC_000005.8:g.56204461C>G NCBI36
NG_031884.1:g.62805C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005921.2:c.1558C>G MANE Select NP_005912.1:p.Gln520Glu
ENST00000399503.4:c.1558C>G MANE Select ENSP00000382423.3:p.Gln520Glu
NM_005921.1:c.1558C>G NP_005912.1:p.Gln520Glu
ENST00000399503.3:c.1558C>G ENSP00000382423.3:p.Gln520Glu
XM_005248519.3:c.1180C>G XP_005248576.2:p.Gln394Glu
XM_011543406.1:c.1303C>G XP_011541708.1:p.Gln435Glu
XM_011543407.1:c.1558C>G XP_011541709.1:p.Gln520Glu
XM_011543408.1:c.1558C>G XP_011541710.1:p.Gln520Glu
XM_017009484.1:c.1147C>G XP_016864973.1:p.Gln383Glu
XM_017009485.1:c.1069C>G XP_016864974.1:p.Gln357Glu
XR_001742068.2:n.1589C>G