Canonical Allele Identifier: CA1548139343
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881876C= , CM000667.2:g.56881876C= GRCh38
NC_000005.9:g.56177703C= , CM000667.1:g.56177703C= GRCh37
NC_000005.8:g.56213460C= NCBI36
NG_031884.1:g.71804C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2676C= MANE Select ENSP00000382423.3:p.Asn892=
ENST00000399503.3:c.2676C= ENSP00000382423.3:p.Asn892=
NM_005921.1:c.2676C= NP_005912.1:p.Asn892=
XM_005248519.3:c.2298C= XP_005248576.2:p.Asn766=
XM_011543406.1:c.2421C= XP_011541708.1:p.Asn807=
XM_011543407.1:c.2397C= XP_011541709.1:p.Asn799=
XM_011543408.1:c.2676C= XP_011541710.1:p.Asn892=
XM_017009484.1:c.2265C= XP_016864973.1:p.Asn755=
XM_017009485.1:c.2187C= XP_016864974.1:p.Asn729=
XR_001742068.2:n.2707C=
NM_005921.2:c.2676C= MANE Select NP_005912.1:p.Asn892=