Canonical Allele Identifier: CA381702155
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.1073A>G ENSP00000435707.3:p.Lys358Arg
ENST00000526780.6:c.1073A>G ENSP00000435668.2:p.Lys358Arg
ENST00000527316.6:c.899A>G ENSP00000435047.2:p.Lys300Arg
ENST00000682708.1:c.1124A>G ENSP00000506866.1:p.Lys375Arg
ENST00000683287.1:c.1109A>G ENSP00000507607.1:p.Lys370Arg
ENST00000683714.1:c.1081A>G ENSP00000508207.1:p.Arg361Gly
ENST00000684396.1:n.1113A>G
ENST00000685320.1:c.488A>G ENSP00000509319.1:p.Lys163Arg
ENST00000690257.1:c.977A>G ENSP00000510750.1:p.Lys326Arg
ENST00000355527.8:c.1073A>G MANE Select ENSP00000347717.4:p.Lys358Arg
ENST00000355527.7:c.1073A>G ENSP00000347717.3:p.Lys358Arg
ENST00000407721.6:c.1073A>G ENSP00000384739.2:p.Lys358Arg
ENST00000525137.1:c.574A>G ENSP00000435956.1:p.Arg192Gly
ENST00000533800.5:c.323A>G ENSP00000435011.1:p.Lys108Arg
ENST00000534795.5:c.319+2082A>G
NM_001163817.1:c.1073A>G NP_001157289.1:p.Lys358Arg
NM_001360.2:c.1073A>G , LRG_340t1:c.1073A>G NP_001351.2:p.Lys358Arg
XM_011544777.1:c.1207A>G XP_011543079.1:p.Arg403Gly
XM_011544777.2:c.1207A>G XP_011543079.1:p.Arg403Gly
NM_001163817.2:c.1073A>G NP_001157289.1:p.Lys358Arg
NM_001360.3:c.1073A>G MANE Select NP_001351.2:p.Lys358Arg