Canonical Allele Identifier: CA290103778
Community Standard Title: NM_001004334.4(GPR179):c.5058C>T (p.Ala1686=)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38328511G>A , CM000679.2:g.38328511G>A GRCh38
NC_000017.9:g.33737920G>A NCBI36
NG_032655.2:g.20300C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.5058C>T MANE Select NP_001004334.3:p.Ala1686=
ENST00000616987.5:c.5058C>T MANE Select ENSP00000483469.2:p.Ala1686=
NM_001004334.3:c.5058C>T NP_001004334.3:p.Ala1686=
ENST00000616987.4:c.5058C>T ENSP00000483469.1:p.Ala1686=
ENST00000621958.1:c.5061C>T ENSP00000480024.1:p.Ala1687=