Canonical Allele Identifier: CA460180813
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs1340477008
gnomAD v2: 8-23540343-C-T
gnomAD v4: 8-23682830-C-T
MyVariant Identifiers: chr8:g.23540343C>T (hg19) chr8:g.23682830C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682830C>T , CM000670.2:g.23682830C>T GRCh38
NC_000008.10:g.23540343C>T , CM000670.1:g.23540343C>T GRCh37
NC_000008.9:g.23596288C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.60G>A MANE Select ENSP00000370253.4:p.Pro20=
ENST00000380871.4:c.60G>A ENSP00000370253.4:p.Pro20=
ENST00000523261.1:c.33+27G>A ENSP00000429729.1:n.33+27G>A
NM_001256339.1:c.33+27G>A NP_001243268.1:n.33+27G>A
NM_006167.3:c.60G>A NP_006158.2:p.Pro20=
NR_046072.1:n.18+74G>A
XR_001745842.1:n.1312+14080C>T
NM_006167.4:c.60G>A MANE Select NP_006158.2:p.Pro20=
NR_046072.2:n.35+74G>A
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