Canonical Allele Identifier: CA460180696
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682773-C-T
MyVariant Identifiers: chr8:g.23540286C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682773C>T , CM000670.2:g.23682773C>T GRCh38
NC_000008.10:g.23540286C>T , CM000670.1:g.23540286C>T GRCh37
NC_000008.9:g.23596231C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.117G>A MANE Select ENSP00000370253.4:p.Ala39=
ENST00000380871.4:c.117G>A ENSP00000370253.4:p.Ala39=
ENST00000523261.1:c.33+84G>A ENSP00000429729.1:n.33+84G>A
NM_001256339.1:c.33+84G>A NP_001243268.1:n.33+84G>A
NM_006167.3:c.117G>A NP_006158.2:p.Ala39=
NR_046072.1:n.18+131G>A
XR_001745842.1:n.1312+14023C>T
NM_006167.4:c.117G>A MANE Select NP_006158.2:p.Ala39=
NR_046072.2:n.35+131G>A
Search 100 bp 5'
Search 100 bp 3'