Canonical Allele Identifier: CA370605274
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs1332416473
gnomAD v3: 8-23682826-G-C
gnomAD v4: 8-23682826-G-C
MyVariant Identifiers: chr8:g.23540339G>C (hg19) chr8:g.23682826G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682826G>C , CM000670.2:g.23682826G>C GRCh38
NC_000008.10:g.23540339G>C , CM000670.1:g.23540339G>C GRCh37
NC_000008.9:g.23596284G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.64C>G MANE Select ENSP00000370253.4:p.Pro22Ala
ENST00000380871.4:c.64C>G ENSP00000370253.4:p.Pro22Ala
ENST00000523261.1:c.33+31C>G ENSP00000429729.1:n.33+31C>G
NM_001256339.1:c.33+31C>G NP_001243268.1:n.33+31C>G
NM_006167.3:c.64C>G NP_006158.2:p.Pro22Ala
NR_046072.1:n.18+78C>G
XR_001745842.1:n.1312+14076G>C
NM_006167.4:c.64C>G MANE Select NP_006158.2:p.Pro22Ala
NR_046072.2:n.35+78C>G
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