Canonical Allele Identifier: CA1981486989
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435730T= , CM000673.2:g.71435730T= GRCh38
NC_000011.9:g.71146776T= , CM000673.1:g.71146776T= GRCh37
NC_000011.8:g.70824424T= NCBI36
NG_012655.2:g.17702A= , LRG_340:g.17702A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.1073A= ENSP00000435707.3:p.Lys358=
ENST00000526780.6:c.1073A= ENSP00000435668.2:p.Lys358=
ENST00000527316.6:c.899A= ENSP00000435047.2:p.Lys300=
ENST00000682708.1:c.1124A= ENSP00000506866.1:p.Lys375=
ENST00000683287.1:c.1109A= ENSP00000507607.1:p.Lys370=
ENST00000683714.1:c.1081A= ENSP00000508207.1:p.Arg361=
ENST00000684396.1:n.1113A=
ENST00000685320.1:c.488A= ENSP00000509319.1:p.Lys163=
ENST00000690257.1:c.977A= ENSP00000510750.1:p.Lys326=
ENST00000355527.8:c.1073A= MANE Select ENSP00000347717.4:p.Lys358=
ENST00000355527.7:c.1073A= ENSP00000347717.3:p.Lys358=
ENST00000407721.6:c.1073A= ENSP00000384739.2:p.Lys358=
ENST00000525137.1:c.574A= ENSP00000435956.1:p.Arg192=
ENST00000533800.5:c.323A= ENSP00000435011.1:p.Lys108=
ENST00000534795.5:c.319+2082A=
NM_001163817.1:c.1073A= NP_001157289.1:p.Lys358=
NM_001360.2:c.1073A= , LRG_340t1:c.1073A= NP_001351.2:p.Lys358=
XM_011544777.1:c.1207A= XP_011543079.1:p.Arg403=
XM_011544777.2:c.1207A= XP_011543079.1:p.Arg403=
NM_001163817.2:c.1073A= NP_001157289.1:p.Lys358=
NM_001360.3:c.1073A= MANE Select NP_001351.2:p.Lys358=