Canonical Allele Identifier: CA8079634
Gene: DRC7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57698010G>A , CM000678.2:g.57698010G>A GRCh38
NC_000016.9:g.57731922G>A , CM000678.1:g.57731922G>A GRCh37
NC_000016.8:g.56289423G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001289162.2:c.61G>A MANE Select NP_001276091.1:p.Glu21Lys
ENST00000360716.8:c.61G>A MANE Select ENSP00000353942.3:p.Glu21Lys
NM_001289162.1:c.61G>A NP_001276091.1:p.Glu21Lys
NM_001289163.1:c.61G>A NP_001276092.1:p.Glu21Lys
NM_001289163.2:c.61G>A NP_001276092.1:p.Glu21Lys
NM_032269.5:c.61G>A NP_115645.4:p.Glu21Lys
NM_032269.6:c.61G>A NP_115645.4:p.Glu21Lys
ENST00000336825.12:c.61G>A ENSP00000338938.8:p.Glu21Lys
ENST00000360716.7:c.61G>A ENSP00000353942.3:p.Glu21Lys
ENST00000394337.8:c.61G>A ENSP00000377869.4:p.Glu21Lys
ENST00000563126.5:c.61G>A ENSP00000457676.1:p.Glu21Lys
ENST00000564297.5:c.61G>A ENSP00000454722.1:p.Glu21Lys
ENST00000569167.1:c.-34+1416G>A ENSP00000455994.1:n.-34+1416G>A
ENST00000569375.5:c.61G>A ENSP00000456441.1:p.Glu21Lys
XM_011523377.1:c.61G>A XP_011521679.1:p.Glu21Lys
XM_011523378.1:c.61G>A XP_011521680.1:p.Glu21Lys