Canonical Allele Identifier: CA1981486917
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435616A= , CM000673.2:g.71435616A= GRCh38
NC_000011.9:g.71146662A= , CM000673.1:g.71146662A= GRCh37
NC_000011.8:g.70824310A= NCBI36
NG_012655.2:g.17816T= , LRG_340:g.17816T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.1187T= ENSP00000435707.3:p.Val396=
ENST00000526780.6:c.1187T= ENSP00000435668.2:p.Val396=
ENST00000527316.6:c.1013T= ENSP00000435047.2:p.Val338=
ENST00000682708.1:c.1238T= ENSP00000506866.1:p.Val413=
ENST00000683287.1:c.1223T= ENSP00000507607.1:p.Val408=
ENST00000683714.1:c.1195T= ENSP00000508207.1:p.Cys399=
ENST00000684396.1:n.1227T=
ENST00000685320.1:c.602T= ENSP00000509319.1:p.Val201=
ENST00000690257.1:c.1091T= ENSP00000510750.1:p.Val364=
ENST00000355527.8:c.1187T= MANE Select ENSP00000347717.4:p.Val396=
ENST00000355527.7:c.1187T= ENSP00000347717.3:p.Val396=
ENST00000407721.6:c.1187T= ENSP00000384739.2:p.Val396=
ENST00000525137.1:c.688T= ENSP00000435956.1:p.Cys230=
ENST00000533800.5:c.437T= ENSP00000435011.1:p.Val146=
ENST00000534795.5:c.319+2196T=
NM_001163817.1:c.1187T= NP_001157289.1:p.Val396=
NM_001360.2:c.1187T= , LRG_340t1:c.1187T= NP_001351.2:p.Val396=
XM_011544777.1:c.1321T= XP_011543079.1:p.Cys441=
XM_011544777.2:c.1321T= XP_011543079.1:p.Cys441=
NM_001163817.2:c.1187T= NP_001157289.1:p.Val396=
NM_001360.3:c.1187T= MANE Select NP_001351.2:p.Val396=