Canonical Allele Identifier: CA12155536
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56887810G>C , CM000667.2:g.56887810G>C GRCh38
NC_000005.9:g.56183637G>C , CM000667.1:g.56183637G>C GRCh37
NC_000005.8:g.56219394G>C NCBI36
NG_031884.1:g.77738G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005921.2:c.4257+290G>C MANE Select NP_005912.1:n.4257+290G>C
ENST00000399503.4:c.4257+290G>C MANE Select ENSP00000382423.3:n.4257+290G>C
NM_005921.1:c.4257+290G>C NP_005912.1:n.4257+290G>C
ENST00000399503.3:c.4257+290G>C ENSP00000382423.3:n.4257+290G>C
ENST00000469188.1:n.544G>C
XM_005248519.3:c.3879+290G>C XP_005248576.2:n.3879+290G>C
XM_011543406.1:c.4002+290G>C XP_011541708.1:n.4002+290G>C
XM_011543407.1:c.3978+290G>C XP_011541709.1:n.3978+290G>C
XM_011543408.1:c.4115-416G>C XP_011541710.1:n.4115-416G>C
XM_017009484.1:c.3846+290G>C XP_016864973.1:n.3846+290G>C
XM_017009485.1:c.3768+290G>C XP_016864974.1:n.3768+290G>C
XR_001742068.2:n.4146-416G>C