Canonical Allele Identifier: CA460180812
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682830-C-G
MyVariant Identifiers: chr8:g.23540343C>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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