Canonical Allele Identifier: CA15386498
Gene: MAP3K1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1017226

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857565T>C , CM000667.2:g.56857565T>C GRCh38
NC_000005.9:g.56153392T>C , CM000667.1:g.56153392T>C GRCh37
NC_000005.8:g.56189149T>C NCBI36
NG_031884.1:g.47493T>C

Transcript Alleles

HGVS Amino-acid change
NM_005921.1:c.633+815T>C VV NP_005912.1:p.=
XM_005248519.3:c.255+815T>C XP_005248576.2:p.=
XM_011543406.1:c.378+815T>C XP_011541708.1:p.=
XM_011543407.1:c.633+815T>C XP_011541709.1:p.=
XM_011543408.1:c.633+815T>C XP_011541710.1:p.=
XM_017009484.1:c.222+815T>C XP_016864973.1:p.=
XM_017009485.1:c.144+815T>C XP_016864974.1:p.=
XR_001742068.2:n.664+815T>C
NM_005921.2:c.633+815T>C VV MANE Preferred NP_005912.1:p.=
ENST00000399503.3:n.633+815T>C ENSP00000382423.3:p.=