Canonical Allele Identifier: CA10645567
Community Standard Title: NM_001004334.4(GPR179):c.3518G>C (p.Ser1173Thr)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38330051C>G , CM000679.2:g.38330051C>G GRCh38
NC_000017.9:g.33739460C>G NCBI36
NG_032655.2:g.18760G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.3518G>C MANE Select NP_001004334.3:p.Ser1173Thr
ENST00000616987.5:c.3518G>C MANE Select ENSP00000483469.2:p.Ser1173Thr
NM_001004334.3:c.3518G>C NP_001004334.3:p.Ser1173Thr
ENST00000616987.4:c.3518G>C ENSP00000483469.1:p.Ser1173Thr
ENST00000621958.1:c.3521G>C ENSP00000480024.1:p.Ser1174Thr