Canonical Allele Identifier: CA370605178
Gene: NKX3-1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23540291C>G (hg19) chr8:g.23682778C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682778C>G , CM000670.2:g.23682778C>G GRCh38
NC_000008.10:g.23540291C>G , CM000670.1:g.23540291C>G GRCh37
NC_000008.9:g.23596236C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.112G>C MANE Select ENSP00000370253.4:p.Gly38Arg
ENST00000380871.4:c.112G>C ENSP00000370253.4:p.Gly38Arg
ENST00000523261.1:c.33+79G>C ENSP00000429729.1:n.33+79G>C
NM_001256339.1:c.33+79G>C NP_001243268.1:n.33+79G>C
NM_006167.3:c.112G>C NP_006158.2:p.Gly38Arg
NR_046072.1:n.18+126G>C
XR_001745842.1:n.1312+14028C>G
NM_006167.4:c.112G>C MANE Select NP_006158.2:p.Gly38Arg
NR_046072.2:n.35+126G>C
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