Canonical Allele Identifier: CA1548139529
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882270A= , CM000667.2:g.56882270A= GRCh38
NC_000005.9:g.56178097A= , CM000667.1:g.56178097A= GRCh37
NC_000005.8:g.56213854A= NCBI36
NG_031884.1:g.72198A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3070A= MANE Select ENSP00000382423.3:p.Lys1024=
ENST00000399503.3:c.3070A= ENSP00000382423.3:p.Lys1024=
NM_005921.1:c.3070A= NP_005912.1:p.Lys1024=
XM_005248519.3:c.2692A= XP_005248576.2:p.Lys898=
XM_011543406.1:c.2815A= XP_011541708.1:p.Lys939=
XM_011543407.1:c.2791A= XP_011541709.1:p.Lys931=
XM_011543408.1:c.3070A= XP_011541710.1:p.Lys1024=
XM_017009484.1:c.2659A= XP_016864973.1:p.Lys887=
XM_017009485.1:c.2581A= XP_016864974.1:p.Lys861=
XR_001742068.2:n.3101A=
NM_005921.2:c.3070A= MANE Select NP_005912.1:p.Lys1024=