Canonical Allele Identifier: CA370605235
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682805-A-G
MyVariant Identifiers: chr8:g.23540318A>G (hg19) chr8:g.23682805A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682805A>G , CM000670.2:g.23682805A>G GRCh38
NC_000008.10:g.23540318A>G , CM000670.1:g.23540318A>G GRCh37
NC_000008.9:g.23596263A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.85T>C MANE Select ENSP00000370253.4:p.Phe29Leu
ENST00000380871.4:c.85T>C ENSP00000370253.4:p.Phe29Leu
ENST00000523261.1:c.33+52T>C ENSP00000429729.1:n.33+52T>C
NM_001256339.1:c.33+52T>C NP_001243268.1:n.33+52T>C
NM_006167.3:c.85T>C NP_006158.2:p.Phe29Leu
NR_046072.1:n.18+99T>C
XR_001745842.1:n.1312+14055A>G
NM_006167.4:c.85T>C MANE Select NP_006158.2:p.Phe29Leu
NR_046072.2:n.35+99T>C
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