Canonical Allele Identifier: CA10649151
Community Standard Title: NM_001004334.4(GPR179):c.6621C>T (p.Ser2207=)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38326948G>A , CM000679.2:g.38326948G>A GRCh38
NC_000017.9:g.33736357G>A NCBI36
NG_032655.2:g.21863C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.6621C>T MANE Select NP_001004334.3:p.Ser2207=
ENST00000616987.5:c.6621C>T MANE Select ENSP00000483469.2:p.Ser2207=
NM_001004334.3:c.6621C>T NP_001004334.3:p.Ser2207=
ENST00000616987.4:c.6621C>T ENSP00000483469.1:p.Ser2207=
ENST00000621958.1:c.6624C>T ENSP00000480024.1:p.Ser2208=
ENST00000622573.1:n.135-1255C>T