Canonical Allele Identifier: CA290110162
Community Standard Title: NM_001004334.4(GPR179):c.858A>G (p.Pro286=)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38339462T>C , CM000679.2:g.38339462T>C GRCh38
NC_000017.9:g.33748871T>C NCBI36
NG_032655.2:g.9349A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.858A>G MANE Select NP_001004334.3:p.Pro286=
ENST00000616987.5:c.858A>G MANE Select ENSP00000483469.2:p.Pro286=
NM_001004334.3:c.858A>G NP_001004334.3:p.Pro286=
ENST00000610867.1:n.916A>G
ENST00000616987.4:c.858A>G ENSP00000483469.1:p.Pro286=
ENST00000621958.1:c.861A>G ENSP00000480024.1:p.Pro287=