Canonical Allele Identifier: CA359787719
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs766945040

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882328C>G , CM000667.2:g.56882328C>G GRCh38
NC_000005.9:g.56178155C>G , CM000667.1:g.56178155C>G GRCh37
NC_000005.8:g.56213912C>G NCBI36
NG_031884.1:g.72256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3128C>G MANE Select ENSP00000382423.3:p.Ser1043Cys
ENST00000399503.3:c.3128C>G ENSP00000382423.3:p.Ser1043Cys
NM_005921.1:c.3128C>G NP_005912.1:p.Ser1043Cys
XM_005248519.3:c.2750C>G XP_005248576.2:p.Ser917Cys
XM_011543406.1:c.2873C>G XP_011541708.1:p.Ser958Cys
XM_011543407.1:c.2849C>G XP_011541709.1:p.Ser950Cys
XM_011543408.1:c.3128C>G XP_011541710.1:p.Ser1043Cys
XM_017009484.1:c.2717C>G XP_016864973.1:p.Ser906Cys
XM_017009485.1:c.2639C>G XP_016864974.1:p.Ser880Cys
XR_001742068.2:n.3159C>G
NM_005921.2:c.3128C>G MANE Select NP_005912.1:p.Ser1043Cys