Canonical Allele Identifier: CA2841098856
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875353dup , CM000667.2:g.56875353dup GRCh38
NC_000005.9:g.56171180dup , CM000667.1:g.56171180dup GRCh37
NC_000005.8:g.56206937dup NCBI36
NG_031884.1:g.65281dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1965+43dup MANE Select ENSP00000382423.3:n.1965+43dup
ENST00000399503.3:c.1965+43dup ENSP00000382423.3:n.1965+43dup
NM_005921.1:c.1965+43dup NP_005912.1:n.1965+43dup
XM_005248519.3:c.1587+43dup XP_005248576.2:n.1587+43dup
XM_011543406.1:c.1710+43dup XP_011541708.1:n.1710+43dup
XM_011543407.1:c.1686+2348dup XP_011541709.1:n.1686+2348dup
XM_011543408.1:c.1965+43dup XP_011541710.1:n.1965+43dup
XM_017009484.1:c.1554+43dup XP_016864973.1:n.1554+43dup
XM_017009485.1:c.1476+43dup XP_016864974.1:n.1476+43dup
XR_001742068.2:n.1996+43dup
NM_005921.2:c.1965+43dup MANE Select NP_005912.1:n.1965+43dup