Canonical Allele Identifier: CA10639557
Community Standard Title: NM_001004334.4(GPR179):c.663G>T (p.Val221=)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38343127C>A , CM000679.2:g.38343127C>A GRCh38
NC_000017.9:g.33752536C>A NCBI36
NG_032655.2:g.5684G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.663G>T MANE Select NP_001004334.3:p.Val221=
ENST00000616987.5:c.663G>T MANE Select ENSP00000483469.2:p.Val221=
NM_001004334.3:c.663G>T NP_001004334.3:p.Val221=
ENST00000610867.1:n.721G>T
ENST00000616987.4:c.663G>T ENSP00000483469.1:p.Val221=
ENST00000621958.1:c.663G>T ENSP00000480024.1:p.Val221=