Canonical Allele Identifier: CA290103567
Community Standard Title: NM_001004334.4(GPR179):c.5416G>A (p.Ala1806Thr)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38328153C>T , CM000679.2:g.38328153C>T GRCh38
NC_000017.9:g.33737562C>T NCBI36
NG_032655.2:g.20658G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.5416G>A MANE Select NP_001004334.3:p.Ala1806Thr
ENST00000616987.5:c.5416G>A MANE Select ENSP00000483469.2:p.Ala1806Thr
NM_001004334.3:c.5416G>A NP_001004334.3:p.Ala1806Thr
ENST00000616987.4:c.5416G>A ENSP00000483469.1:p.Ala1806Thr
ENST00000621958.1:c.5419G>A ENSP00000480024.1:p.Ala1807Thr
ENST00000622573.1:n.134+217G>A