Canonical Allele Identifier: CA370605253
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs1563298304
gnomAD v3: 8-23682816-G-A
gnomAD v4: 8-23682816-G-A
MyVariant Identifiers: chr8:g.23540329G>A (hg19) chr8:g.23682816G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682816G>A , CM000670.2:g.23682816G>A GRCh38
NC_000008.10:g.23540329G>A , CM000670.1:g.23540329G>A GRCh37
NC_000008.9:g.23596274G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.74C>T MANE Select ENSP00000370253.4:p.Pro25Leu
ENST00000380871.4:c.74C>T ENSP00000370253.4:p.Pro25Leu
ENST00000523261.1:c.33+41C>T ENSP00000429729.1:n.33+41C>T
NM_001256339.1:c.33+41C>T NP_001243268.1:n.33+41C>T
NM_006167.3:c.74C>T NP_006158.2:p.Pro25Leu
NR_046072.1:n.18+88C>T
XR_001745842.1:n.1312+14066G>A
NM_006167.4:c.74C>T MANE Select NP_006158.2:p.Pro25Leu
NR_046072.2:n.35+88C>T
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