Canonical Allele Identifier: CA1548139437
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1748231265

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882072dup , CM000667.2:g.56882072dup GRCh38
NC_000005.9:g.56177899dup , CM000667.1:g.56177899dup GRCh37
NC_000005.8:g.56213656dup NCBI36
NG_031884.1:g.72000dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2872dup MANE Select ENSP00000382423.3:p.Thr958AsnfsTer?
ENST00000399503.3:c.2872dup ENSP00000382423.3:p.Thr958AsnfsTer?
NM_005921.1:c.2872dup NP_005912.1:p.Thr958AsnfsTer?
XM_005248519.3:c.2494dup XP_005248576.2:p.Thr832AsnfsTer?
XM_011543406.1:c.2617dup XP_011541708.1:p.Thr873AsnfsTer?
XM_011543407.1:c.2593dup XP_011541709.1:p.Thr865AsnfsTer?
XM_011543408.1:c.2872dup XP_011541710.1:p.Thr958AsnfsTer?
XM_017009484.1:c.2461dup XP_016864973.1:p.Thr821AsnfsTer?
XM_017009485.1:c.2383dup XP_016864974.1:p.Thr795AsnfsTer?
XR_001742068.2:n.2903dup
NM_005921.2:c.2872dup MANE Select NP_005912.1:p.Thr958AsnfsTer?