Canonical Allele Identifier: CA359786019
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111941500

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881740C>T , CM000667.2:g.56881740C>T GRCh38
NC_000005.9:g.56177567C>T , CM000667.1:g.56177567C>T GRCh37
NC_000005.8:g.56213324C>T NCBI36
NG_031884.1:g.71668C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2540C>T MANE Select ENSP00000382423.3:p.Thr847Ile
ENST00000399503.3:c.2540C>T ENSP00000382423.3:p.Thr847Ile
NM_005921.1:c.2540C>T NP_005912.1:p.Thr847Ile
XM_005248519.3:c.2162C>T XP_005248576.2:p.Thr721Ile
XM_011543406.1:c.2285C>T XP_011541708.1:p.Thr762Ile
XM_011543407.1:c.2261C>T XP_011541709.1:p.Thr754Ile
XM_011543408.1:c.2540C>T XP_011541710.1:p.Thr847Ile
XM_017009484.1:c.2129C>T XP_016864973.1:p.Thr710Ile
XM_017009485.1:c.2051C>T XP_016864974.1:p.Thr684Ile
XR_001742068.2:n.2571C>T
NM_005921.2:c.2540C>T MANE Select NP_005912.1:p.Thr847Ile