Canonical Allele Identifier: CA1548128117
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1579751170

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857436A>C , CM000667.2:g.56857436A>C GRCh38
NC_000005.9:g.56153263A>C , CM000667.1:g.56153263A>C GRCh37
NC_000005.8:g.56189020A>C NCBI36
NG_031884.1:g.47364A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.633+686A>C MANE Select ENSP00000382423.3:n.633+686A>C
ENST00000399503.3:c.633+686A>C ENSP00000382423.3:n.633+686A>C
NM_005921.1:c.633+686A>C NP_005912.1:n.633+686A>C
XM_005248519.3:c.255+686A>C XP_005248576.2:n.255+686A>C
XM_011543406.1:c.378+686A>C XP_011541708.1:n.378+686A>C
XM_011543407.1:c.633+686A>C XP_011541709.1:n.633+686A>C
XM_011543408.1:c.633+686A>C XP_011541710.1:n.633+686A>C
XM_017009484.1:c.222+686A>C XP_016864973.1:n.222+686A>C
XM_017009485.1:c.144+686A>C XP_016864974.1:n.144+686A>C
XR_001742068.2:n.664+686A>C
NM_005921.2:c.633+686A>C MANE Select NP_005912.1:n.633+686A>C