Canonical Allele Identifier: CA1548139438
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882077A= , CM000667.2:g.56882077A= GRCh38
NC_000005.9:g.56177904A= , CM000667.1:g.56177904A= GRCh37
NC_000005.8:g.56213661A= NCBI36
NG_031884.1:g.72005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2877A= MANE Select ENSP00000382423.3:p.Lys959=
ENST00000399503.3:c.2877A= ENSP00000382423.3:p.Lys959=
NM_005921.1:c.2877A= NP_005912.1:p.Lys959=
XM_005248519.3:c.2499A= XP_005248576.2:p.Lys833=
XM_011543406.1:c.2622A= XP_011541708.1:p.Lys874=
XM_011543407.1:c.2598A= XP_011541709.1:p.Lys866=
XM_011543408.1:c.2877A= XP_011541710.1:p.Lys959=
XM_017009484.1:c.2466A= XP_016864973.1:p.Lys822=
XM_017009485.1:c.2388A= XP_016864974.1:p.Lys796=
XR_001742068.2:n.2908A=
NM_005921.2:c.2877A= MANE Select NP_005912.1:p.Lys959=