Canonical Allele Identifier: CA370605246
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682813-A-C
MyVariant Identifiers: chr8:g.23540326A>C (hg19) chr8:g.23682813A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682813A>C , CM000670.2:g.23682813A>C GRCh38
NC_000008.10:g.23540326A>C , CM000670.1:g.23540326A>C GRCh37
NC_000008.9:g.23596271A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.77T>G MANE Select ENSP00000370253.4:p.Leu26Arg
ENST00000380871.4:c.77T>G ENSP00000370253.4:p.Leu26Arg
ENST00000523261.1:c.33+44T>G ENSP00000429729.1:n.33+44T>G
NM_001256339.1:c.33+44T>G NP_001243268.1:n.33+44T>G
NM_006167.3:c.77T>G NP_006158.2:p.Leu26Arg
NR_046072.1:n.18+91T>G
XR_001745842.1:n.1312+14063A>C
NM_006167.4:c.77T>G MANE Select NP_006158.2:p.Leu26Arg
NR_046072.2:n.35+91T>G
Search 100 bp 5'
Search 100 bp 3'