Canonical Allele Identifier: CA1771026959
Gene: NKX3-1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682766G= , CM000670.2:g.23682766G= GRCh38
NC_000008.10:g.23540279G= , CM000670.1:g.23540279G= GRCh37
NC_000008.9:g.23596224G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.124C= MANE Select ENSP00000370253.4:p.Gln42=
ENST00000380871.4:c.124C= ENSP00000370253.4:p.Gln42=
ENST00000523261.1:c.33+91C= ENSP00000429729.1:n.33+91C=
NM_001256339.1:c.33+91C= NP_001243268.1:n.33+91C=
NM_006167.3:c.124C= NP_006158.2:p.Gln42=
NR_046072.1:n.18+138C=
XR_001745842.1:n.1312+14016G=
NM_006167.4:c.124C= MANE Select NP_006158.2:p.Gln42=
NR_046072.2:n.35+138C=