Canonical Allele Identifier: CA1771027012
Gene: NKX3-1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682793C= , CM000670.2:g.23682793C= GRCh38
NC_000008.10:g.23540306C= , CM000670.1:g.23540306C= GRCh37
NC_000008.9:g.23596251C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.97G= MANE Select ENSP00000370253.4:p.Asp33=
ENST00000380871.4:c.97G= ENSP00000370253.4:p.Asp33=
ENST00000523261.1:c.33+64G= ENSP00000429729.1:n.33+64G=
NM_001256339.1:c.33+64G= NP_001243268.1:n.33+64G=
NM_006167.3:c.97G= NP_006158.2:p.Asp33=
NR_046072.1:n.18+111G=
XR_001745842.1:n.1312+14043C=
NM_006167.4:c.97G= MANE Select NP_006158.2:p.Asp33=
NR_046072.2:n.35+111G=