Canonical Allele Identifier: CA129748
Community Standard Title: NM_001004334.4(GPR179):c.598C>T (p.Arg200Ter)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38343192G>A , CM000679.2:g.38343192G>A GRCh38
NC_000017.9:g.33752601G>A NCBI36
NG_032655.2:g.5619C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.598C>T MANE Select NP_001004334.3:p.Arg200Ter
ENST00000616987.5:c.598C>T MANE Select ENSP00000483469.2:p.Arg200Ter
NM_001004334.3:c.598C>T NP_001004334.3:p.Arg200Ter
ENST00000610867.1:n.656C>T
ENST00000616987.4:c.598C>T ENSP00000483469.1:p.Arg200Ter
ENST00000621958.1:c.598C>T ENSP00000480024.1:p.Arg200Ter