Canonical Allele Identifier: CA1548128172
Community Standard Title: NM_005921.2(MAP3K1):c.633+815T=
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857565T= , CM000667.2:g.56857565T= GRCh38
NC_000005.9:g.56153392T= , CM000667.1:g.56153392T= GRCh37
NC_000005.8:g.56189149T= NCBI36
NG_031884.1:g.47493T=

Transcript Alleles

HGVS Amino-acid Change
NM_005921.2:c.633+815T= MANE Select NP_005912.1:n.633+815T=
ENST00000399503.4:c.633+815T= MANE Select ENSP00000382423.3:n.633+815T=
NM_005921.1:c.633+815T= NP_005912.1:n.633+815T=
ENST00000399503.3:c.633+815T= ENSP00000382423.3:n.633+815T=
XM_005248519.3:c.255+815T= XP_005248576.2:n.255+815T=
XM_011543406.1:c.378+815T= XP_011541708.1:n.378+815T=
XM_011543407.1:c.633+815T= XP_011541709.1:n.633+815T=
XM_011543408.1:c.633+815T= XP_011541710.1:n.633+815T=
XM_017009484.1:c.222+815T= XP_016864973.1:n.222+815T=
XM_017009485.1:c.144+815T= XP_016864974.1:n.144+815T=
XR_001742068.2:n.664+815T=