Canonical Allele Identifier: CA580953548

Gene: NKX3-1

Linked Data

• dbSNP Id: rs1563298238
• gnomAD v2: 8-23540266-G-GTGCGGCCGCCTTGCC
• gnomAD v4: 8-23682753-G-GTGCGGCCGCCTTGCC
• MyVariant Identifiers: chr8:g.23540266_23540267insTGCGGCCGCCTTGCC (hg19) ; chr8:g.23682753_23682754insTGCGGCCGCCTTGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23682754_23682768dup , CM000670.2:g.23682754_23682768dup	GRCh38
NC_000008.10:g.23540267_23540281dup , CM000670.1:g.23540267_23540281dup	GRCh37
NC_000008.9:g.23596212_23596226dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380871.5:c.122_136dup MANE Select	ENSP00000370253.4:p.Arg45_Thr46insArgGlnGlyGlyArg
ENST00000380871.4:c.122_136dup	ENSP00000370253.4:p.Arg45_Thr46insArgGlnGlyGlyArg
ENST00000523261.1:c.33+89_33+103dup	ENSP00000429729.1:n.33+89_33+103dup
NM_001256339.1:c.33+89_33+103dup	NP_001243268.1:n.33+89_33+103dup
NM_006167.3:c.122_136dup	NP_006158.2:p.Arg45_Thr46insArgGlnGlyGlyArg
NR_046072.1:n.18+136_18+150dup
XR_001745842.1:n.1312+14004_1312+14018dup
NM_006167.4:c.122_136dup MANE Select	NP_006158.2:p.Arg45_Thr46insArgGlnGlyGlyArg
NR_046072.2:n.35+136_35+150dup