Canonical Allele Identifier: CA2976951424
Community Standard Title: NM_001360.3(DHCR7):c.858del (p.Trp286Ter)
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71437918del , CM000673.2:g.71437918del GRCh38
NC_000011.9:g.71148964del , CM000673.1:g.71148964del GRCh37
NC_000011.8:g.70826612del NCBI36
NG_012655.2:g.15515del , LRG_340:g.15515del

Transcript Alleles

HGVS Amino-acid Change
NM_001360.3:c.858del MANE Select NP_001351.2:p.Trp286Ter
ENST00000355527.8:c.858del MANE Select ENSP00000347717.4:p.Trp286Ter
NM_001163817.1:c.858del NP_001157289.1:p.Trp286Ter
NM_001163817.2:c.858del NP_001157289.1:p.Trp286Ter
NM_001360.2:c.858del , LRG_340t1:c.858del NP_001351.2:p.Trp286Ter
ENST00000355527.7:c.858del ENSP00000347717.3:p.Trp286Ter
ENST00000407721.6:c.858del ENSP00000384739.2:p.Trp286Ter
ENST00000525137.1:c.225del ENSP00000435956.1:p.Trp75Ter
ENST00000525346.6:c.858del ENSP00000435707.3:p.Trp286Ter
ENST00000526780.6:c.858del ENSP00000435668.2:p.Trp286Ter
ENST00000527316.5:c.762del ENSP00000435047.1:p.Trp254Ter
ENST00000527316.6:c.684del ENSP00000435047.2:p.Trp228Ter
ENST00000533800.5:c.108del ENSP00000435011.1:p.Trp36Ter
ENST00000534795.5:c.214del
ENST00000682708.1:c.909del ENSP00000506866.1:p.Trp303Ter
ENST00000682880.1:c.858del ENSP00000507520.1:p.Trp286Ter
ENST00000683287.1:c.894del ENSP00000507607.1:p.Trp298Ter
ENST00000683714.1:c.858del ENSP00000508207.1:p.Trp286Ter
ENST00000684396.1:n.898del
ENST00000685320.1:c.273del ENSP00000509319.1:p.Trp91Ter
ENST00000690257.1:c.762del ENSP00000510750.1:p.Trp254Ter
XM_011544777.1:c.858del XP_011543079.1:p.Trp286Ter
XM_011544777.2:c.858del XP_011543079.1:p.Trp286Ter