Canonical Allele Identifier: CA398879992
Community Standard Title: NM_001004334.4(GPR179):c.3349G>C (p.Gly1117Arg)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38330220C>G , CM000679.2:g.38330220C>G GRCh38
NC_000017.9:g.33739629C>G NCBI36
NG_032655.2:g.18591G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.3349G>C MANE Select NP_001004334.3:p.Gly1117Arg
ENST00000616987.5:c.3349G>C MANE Select ENSP00000483469.2:p.Gly1117Arg
NM_001004334.3:c.3349G>C NP_001004334.3:p.Gly1117Arg
ENST00000616987.4:c.3349G>C ENSP00000483469.1:p.Gly1117Arg
ENST00000621958.1:c.3352G>C ENSP00000480024.1:p.Gly1118Arg