Canonical Allele Identifier: CA10639545
Community Standard Title: NM_001004334.4(GPR179):c.6335C>T (p.Ala2112Val)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38327234G>A , CM000679.2:g.38327234G>A GRCh38
NC_000017.9:g.33736643G>A NCBI36
NG_032655.2:g.21577C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.6335C>T MANE Select NP_001004334.3:p.Ala2112Val
ENST00000616987.5:c.6335C>T MANE Select ENSP00000483469.2:p.Ala2112Val
NM_001004334.3:c.6335C>T NP_001004334.3:p.Ala2112Val
ENST00000616987.4:c.6335C>T ENSP00000483469.1:p.Ala2112Val
ENST00000621958.1:c.6338C>T ENSP00000480024.1:p.Ala2113Val
ENST00000622573.1:n.134+1136C>T