Canonical Allele Identifier: CA359802581
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859846C>G , CM000667.2:g.56859846C>G GRCh38
NC_000005.9:g.56155673C>G , CM000667.1:g.56155673C>G GRCh37
NC_000005.8:g.56191430C>G NCBI36
NG_031884.1:g.49774C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.765C>G MANE Select ENSP00000382423.3:p.Asn255Lys
ENST00000399503.3:c.765C>G ENSP00000382423.3:p.Asn255Lys
NM_005921.1:c.765C>G NP_005912.1:p.Asn255Lys
XM_005248519.3:c.387C>G XP_005248576.2:p.Asn129Lys
XM_011543406.1:c.510C>G XP_011541708.1:p.Asn170Lys
XM_011543407.1:c.765C>G XP_011541709.1:p.Asn255Lys
XM_011543408.1:c.765C>G XP_011541710.1:p.Asn255Lys
XM_017009484.1:c.354C>G XP_016864973.1:p.Asn118Lys
XM_017009485.1:c.276C>G XP_016864974.1:p.Asn92Lys
XR_001742068.2:n.796C>G
NM_005921.2:c.765C>G MANE Select NP_005912.1:p.Asn255Lys