Canonical Allele Identifier: CA370605208

Gene: NKX3-1

Linked Data

• gnomAD v4: 8-23682793-C-A
• MyVariant Identifiers: chr8:g.23540306C>A (hg19) ; chr8:g.23682793C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23682793C>A , CM000670.2:g.23682793C>A	GRCh38
NC_000008.10:g.23540306C>A , CM000670.1:g.23540306C>A	GRCh37
NC_000008.9:g.23596251C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380871.5:c.97G>T MANE Select	ENSP00000370253.4:p.Asp33Tyr
ENST00000380871.4:c.97G>T	ENSP00000370253.4:p.Asp33Tyr
ENST00000523261.1:c.33+64G>T	ENSP00000429729.1:n.33+64G>T
NM_001256339.1:c.33+64G>T	NP_001243268.1:n.33+64G>T
NM_006167.3:c.97G>T	NP_006158.2:p.Asp33Tyr
NR_046072.1:n.18+111G>T
XR_001745842.1:n.1312+14043C>A
NM_006167.4:c.97G>T MANE Select	NP_006158.2:p.Asp33Tyr
NR_046072.2:n.35+111G>T