Canonical Allele Identifier: CA1981486834
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435465C= , CM000673.2:g.71435465C= GRCh38
NC_000011.9:g.71146511C= , CM000673.1:g.71146511C= GRCh37
NC_000011.8:g.70824159C= NCBI36
NG_012655.2:g.17967G= , LRG_340:g.17967G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.1338G= ENSP00000435707.3:p.Arg446=
ENST00000526780.6:c.1338G= ENSP00000435668.2:p.Arg446=
ENST00000527316.6:c.1164G= ENSP00000435047.2:p.Arg388=
ENST00000682708.1:c.1389G= ENSP00000506866.1:p.Arg463=
ENST00000683287.1:c.1374G= ENSP00000507607.1:p.Arg458=
ENST00000683714.1:c.*101G= ENSP00000508207.1:n.*101G=
ENST00000684396.1:n.1378G=
ENST00000685320.1:c.753G= ENSP00000509319.1:p.Arg251=
ENST00000690257.1:c.1242G= ENSP00000510750.1:p.Arg414=
ENST00000355527.8:c.1338G= MANE Select ENSP00000347717.4:p.Arg446=
ENST00000355527.7:c.1338G= ENSP00000347717.3:p.Arg446=
ENST00000407721.6:c.1338G= ENSP00000384739.2:p.Arg446=
ENST00000525137.1:c.839G= ENSP00000435956.1:n.839G=
ENST00000533800.5:c.588G= ENSP00000435011.1:p.Arg196=
ENST00000534795.5:c.319+2347G=
NM_001163817.1:c.1338G= NP_001157289.1:p.Arg446=
NM_001360.2:c.1338G= , LRG_340t1:c.1338G= NP_001351.2:p.Arg446=
XM_011544777.1:c.*101G= XP_011543079.1:n.*101G=
XM_011544777.2:c.*101G= XP_011543079.1:n.*101G=
NM_001163817.2:c.1338G= NP_001157289.1:p.Arg446=
NM_001360.3:c.1338G= MANE Select NP_001351.2:p.Arg446=