Canonical Allele Identifier: CA1981486987
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435729C= , CM000673.2:g.71435729C= GRCh38
NC_000011.9:g.71146775C= , CM000673.1:g.71146775C= GRCh37
NC_000011.8:g.70824423C= NCBI36
NG_012655.2:g.17703G= , LRG_340:g.17703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.1074G= ENSP00000435707.3:p.Lys358=
ENST00000526780.6:c.1074G= ENSP00000435668.2:p.Lys358=
ENST00000527316.6:c.900G= ENSP00000435047.2:p.Lys300=
ENST00000682708.1:c.1125G= ENSP00000506866.1:p.Lys375=
ENST00000683287.1:c.1110G= ENSP00000507607.1:p.Lys370=
ENST00000683714.1:c.1082G= ENSP00000508207.1:p.Arg361=
ENST00000684396.1:n.1114G=
ENST00000685320.1:c.489G= ENSP00000509319.1:p.Lys163=
ENST00000690257.1:c.978G= ENSP00000510750.1:p.Lys326=
ENST00000355527.8:c.1074G= MANE Select ENSP00000347717.4:p.Lys358=
ENST00000355527.7:c.1074G= ENSP00000347717.3:p.Lys358=
ENST00000407721.6:c.1074G= ENSP00000384739.2:p.Lys358=
ENST00000525137.1:c.575G= ENSP00000435956.1:p.Arg192=
ENST00000533800.5:c.324G= ENSP00000435011.1:p.Lys108=
ENST00000534795.5:c.319+2083G=
NM_001163817.1:c.1074G= NP_001157289.1:p.Lys358=
NM_001360.2:c.1074G= , LRG_340t1:c.1074G= NP_001351.2:p.Lys358=
XM_011544777.1:c.1208G= XP_011543079.1:p.Arg403=
XM_011544777.2:c.1208G= XP_011543079.1:p.Arg403=
NM_001163817.2:c.1074G= NP_001157289.1:p.Lys358=
NM_001360.3:c.1074G= MANE Select NP_001351.2:p.Lys358=