Canonical Allele Identifier: CA1771026970
Gene: NKX3-1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682771T= , CM000670.2:g.23682771T= GRCh38
NC_000008.10:g.23540284T= , CM000670.1:g.23540284T= GRCh37
NC_000008.9:g.23596229T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.119A= MANE Select ENSP00000370253.4:p.Gln40=
ENST00000380871.4:c.119A= ENSP00000370253.4:p.Gln40=
ENST00000523261.1:c.33+86A= ENSP00000429729.1:n.33+86A=
NM_001256339.1:c.33+86A= NP_001243268.1:n.33+86A=
NM_006167.3:c.119A= NP_006158.2:p.Gln40=
NR_046072.1:n.18+133A=
XR_001745842.1:n.1312+14021T=
NM_006167.4:c.119A= MANE Select NP_006158.2:p.Gln40=
NR_046072.2:n.35+133A=