Canonical Allele Identifier: CA370605111
Gene: NKX3-1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682742T>A , CM000670.2:g.23682742T>A GRCh38
NC_000008.10:g.23540255T>A , CM000670.1:g.23540255T>A GRCh37
NC_000008.9:g.23596200T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.148A>T MANE Select ENSP00000370253.4:p.Arg50Ter
ENST00000380871.4:c.148A>T ENSP00000370253.4:p.Arg50Ter
ENST00000523261.1:c.34-111A>T ENSP00000429729.1:n.34-111A>T
NM_001256339.1:c.34-111A>T NP_001243268.1:n.34-111A>T
NM_006167.3:c.148A>T NP_006158.2:p.Arg50Ter
NR_046072.1:n.18+162A>T
XR_001745842.1:n.1312+13992T>A
NM_006167.4:c.148A>T MANE Select NP_006158.2:p.Arg50Ter
NR_046072.2:n.35+162A>T