Canonical Allele Identifier: CA460180801
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682824-C-A
MyVariant Identifiers: chr8:g.23540337C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682824C>A , CM000670.2:g.23682824C>A GRCh38
NC_000008.10:g.23540337C>A , CM000670.1:g.23540337C>A GRCh37
NC_000008.9:g.23596282C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.66G>T MANE Select ENSP00000370253.4:p.Pro22=
ENST00000380871.4:c.66G>T ENSP00000370253.4:p.Pro22=
ENST00000523261.1:c.33+33G>T ENSP00000429729.1:n.33+33G>T
NM_001256339.1:c.33+33G>T NP_001243268.1:n.33+33G>T
NM_006167.3:c.66G>T NP_006158.2:p.Pro22=
NR_046072.1:n.18+80G>T
XR_001745842.1:n.1312+14074C>A
NM_006167.4:c.66G>T MANE Select NP_006158.2:p.Pro22=
NR_046072.2:n.35+80G>T