Canonical Allele Identifier: CA444398897
Gene: MAP3K1 HGNC NCBI

Linked Data

gnomAD v4: 5-56875098-A-C
MyVariant Identifiers: chr5:g.56170925A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875098A>C , CM000667.2:g.56875098A>C GRCh38
NC_000005.9:g.56170925A>C , CM000667.1:g.56170925A>C GRCh37
NC_000005.8:g.56206682A>C NCBI36
NG_031884.1:g.65026A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1753A>C MANE Select ENSP00000382423.3:p.Arg585=
ENST00000399503.3:c.1753A>C ENSP00000382423.3:p.Arg585=
NM_005921.1:c.1753A>C NP_005912.1:p.Arg585=
XM_005248519.3:c.1375A>C XP_005248576.2:p.Arg459=
XM_011543406.1:c.1498A>C XP_011541708.1:p.Arg500=
XM_011543407.1:c.1686+2093A>C XP_011541709.1:n.1686+2093A>C
XM_011543408.1:c.1753A>C XP_011541710.1:p.Arg585=
XM_017009484.1:c.1342A>C XP_016864973.1:p.Arg448=
XM_017009485.1:c.1264A>C XP_016864974.1:p.Arg422=
XR_001742068.2:n.1784A>C
NM_005921.2:c.1753A>C MANE Select NP_005912.1:p.Arg585=