Canonical Allele Identifier: CA370605184

Gene: NKX3-1

Linked Data

• gnomAD v4: 8-23682780-T-C
• COSMIC: COSM6362381
• MyVariant Identifiers: chr8:g.23540293T>C (hg19) ; chr8:g.23682780T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23682780T>C , CM000670.2:g.23682780T>C	GRCh38
NC_000008.10:g.23540293T>C , CM000670.1:g.23540293T>C	GRCh37
NC_000008.9:g.23596238T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380871.5:c.110A>G MANE Select	ENSP00000370253.4:p.Asp37Gly
ENST00000380871.4:c.110A>G	ENSP00000370253.4:p.Asp37Gly
ENST00000523261.1:c.33+77A>G	ENSP00000429729.1:n.33+77A>G
NM_001256339.1:c.33+77A>G	NP_001243268.1:n.33+77A>G
NM_006167.3:c.110A>G	NP_006158.2:p.Asp37Gly
NR_046072.1:n.18+124A>G
XR_001745842.1:n.1312+14030T>C
NM_006167.4:c.110A>G MANE Select	NP_006158.2:p.Asp37Gly
NR_046072.2:n.35+124A>G