Canonical Allele Identifier: CA444399181
Gene: MAP3K1 HGNC NCBI

Linked Data

gnomAD v4: 5-56881858-G-A
MyVariant Identifiers: chr5:g.56177685G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881858G>A , CM000667.2:g.56881858G>A GRCh38
NC_000005.9:g.56177685G>A , CM000667.1:g.56177685G>A GRCh37
NC_000005.8:g.56213442G>A NCBI36
NG_031884.1:g.71786G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2658G>A MANE Select ENSP00000382423.3:p.Gln886=
ENST00000399503.3:c.2658G>A ENSP00000382423.3:p.Gln886=
NM_005921.1:c.2658G>A NP_005912.1:p.Gln886=
XM_005248519.3:c.2280G>A XP_005248576.2:p.Gln760=
XM_011543406.1:c.2403G>A XP_011541708.1:p.Gln801=
XM_011543407.1:c.2379G>A XP_011541709.1:p.Gln793=
XM_011543408.1:c.2658G>A XP_011541710.1:p.Gln886=
XM_017009484.1:c.2247G>A XP_016864973.1:p.Gln749=
XM_017009485.1:c.2169G>A XP_016864974.1:p.Gln723=
XR_001742068.2:n.2689G>A
NM_005921.2:c.2658G>A MANE Select NP_005912.1:p.Gln886=