Canonical Allele Identifier: CA460180775
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682812-G-T
MyVariant Identifiers: chr8:g.23540325G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682812G>T , CM000670.2:g.23682812G>T GRCh38
NC_000008.10:g.23540325G>T , CM000670.1:g.23540325G>T GRCh37
NC_000008.9:g.23596270G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.78C>A MANE Select ENSP00000370253.4:p.Leu26=
ENST00000380871.4:c.78C>A ENSP00000370253.4:p.Leu26=
ENST00000523261.1:c.33+45C>A ENSP00000429729.1:n.33+45C>A
NM_001256339.1:c.33+45C>A NP_001243268.1:n.33+45C>A
NM_006167.3:c.78C>A NP_006158.2:p.Leu26=
NR_046072.1:n.18+92C>A
XR_001745842.1:n.1312+14062G>T
NM_006167.4:c.78C>A MANE Select NP_006158.2:p.Leu26=
NR_046072.2:n.35+92C>A
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