Canonical Allele Identifier: CA10645551
Community Standard Title: NM_001004334.4(GPR179):c.5350C>A (p.Pro1784Thr)
Gene: GPR179 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38328219G>T , CM000679.2:g.38328219G>T GRCh38
NC_000017.9:g.33737628G>T NCBI36
NG_032655.2:g.20592C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.5350C>A MANE Select NP_001004334.3:p.Pro1784Thr
ENST00000616987.5:c.5350C>A MANE Select ENSP00000483469.2:p.Pro1784Thr
NM_001004334.3:c.5350C>A NP_001004334.3:p.Pro1784Thr
ENST00000616987.4:c.5350C>A ENSP00000483469.1:p.Pro1784Thr
ENST00000621958.1:c.5353C>A ENSP00000480024.1:p.Pro1785Thr
ENST00000622573.1:n.134+151C>A
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