Canonical Allele Identifier: CA359786438
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881900T>G , CM000667.2:g.56881900T>G GRCh38
NC_000005.9:g.56177727T>G , CM000667.1:g.56177727T>G GRCh37
NC_000005.8:g.56213484T>G NCBI36
NG_031884.1:g.71828T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2700T>G MANE Select ENSP00000382423.3:p.Ser900Arg
ENST00000399503.3:c.2700T>G ENSP00000382423.3:p.Ser900Arg
NM_005921.1:c.2700T>G NP_005912.1:p.Ser900Arg
XM_005248519.3:c.2322T>G XP_005248576.2:p.Ser774Arg
XM_011543406.1:c.2445T>G XP_011541708.1:p.Ser815Arg
XM_011543407.1:c.2421T>G XP_011541709.1:p.Ser807Arg
XM_011543408.1:c.2700T>G XP_011541710.1:p.Ser900Arg
XM_017009484.1:c.2289T>G XP_016864973.1:p.Ser763Arg
XM_017009485.1:c.2211T>G XP_016864974.1:p.Ser737Arg
XR_001742068.2:n.2731T>G
NM_005921.2:c.2700T>G MANE Select NP_005912.1:p.Ser900Arg