Canonical Allele Identifier: CA359786322
Gene: MAP3K1 HGNC NCBI

Linked Data

gnomAD v4: 5-56881871-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881871A>C , CM000667.2:g.56881871A>C GRCh38
NC_000005.9:g.56177698A>C , CM000667.1:g.56177698A>C GRCh37
NC_000005.8:g.56213455A>C NCBI36
NG_031884.1:g.71799A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2671A>C MANE Select ENSP00000382423.3:p.Asn891His
ENST00000399503.3:c.2671A>C ENSP00000382423.3:p.Asn891His
NM_005921.1:c.2671A>C NP_005912.1:p.Asn891His
XM_005248519.3:c.2293A>C XP_005248576.2:p.Asn765His
XM_011543406.1:c.2416A>C XP_011541708.1:p.Asn806His
XM_011543407.1:c.2392A>C XP_011541709.1:p.Asn798His
XM_011543408.1:c.2671A>C XP_011541710.1:p.Asn891His
XM_017009484.1:c.2260A>C XP_016864973.1:p.Asn754His
XM_017009485.1:c.2182A>C XP_016864974.1:p.Asn728His
XR_001742068.2:n.2702A>C
NM_005921.2:c.2671A>C MANE Select NP_005912.1:p.Asn891His