Canonical Allele Identifier: CA10639556
Community Standard Title: NM_001004334.4(GPR179):c.691C>T (p.Pro231Ser)
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38343099G>A , CM000679.2:g.38343099G>A GRCh38
NC_000017.9:g.33752508G>A NCBI36
NG_032655.2:g.5712C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.691C>T MANE Select NP_001004334.3:p.Pro231Ser
ENST00000616987.5:c.691C>T MANE Select ENSP00000483469.2:p.Pro231Ser
NM_001004334.3:c.691C>T NP_001004334.3:p.Pro231Ser
ENST00000610867.1:n.749C>T
ENST00000616987.4:c.691C>T ENSP00000483469.1:p.Pro231Ser
ENST00000621958.1:c.691C>T ENSP00000480024.1:p.Pro231Ser