Canonical Allele Identifier: CA1981487538
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71436852T= , CM000673.2:g.71436852T= GRCh38
NC_000011.9:g.71147898T= , CM000673.1:g.71147898T= GRCh37
NC_000011.8:g.70825546T= NCBI36
NG_012655.2:g.16580A= , LRG_340:g.16580A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.963+960A= ENSP00000435707.3:n.963+960A=
ENST00000526780.6:c.963+960A= ENSP00000435668.2:n.963+960A=
ENST00000527316.6:c.789+960A= ENSP00000435047.2:n.789+960A=
ENST00000682708.1:c.1014+960A= ENSP00000506866.1:n.1014+960A=
ENST00000682880.1:c.*822A= ENSP00000507520.1:n.*822A=
ENST00000683287.1:c.999+960A= ENSP00000507607.1:n.999+960A=
ENST00000683714.1:c.971+952A= ENSP00000508207.1:n.971+952A=
ENST00000684396.1:n.1003+960A=
ENST00000685320.1:c.378+960A= ENSP00000509319.1:n.378+960A=
ENST00000690257.1:c.867+960A= ENSP00000510750.1:n.867+960A=
ENST00000355527.8:c.963+960A= MANE Select ENSP00000347717.4:n.963+960A=
ENST00000355527.7:c.963+960A= ENSP00000347717.3:n.963+960A=
ENST00000407721.6:c.963+960A= ENSP00000384739.2:n.963+960A=
ENST00000525137.1:c.331-879A= ENSP00000435956.1:n.331-879A=
ENST00000533800.5:c.213+960A= ENSP00000435011.1:n.213+960A=
ENST00000534795.5:c.319+960A=
NM_001163817.1:c.963+960A= NP_001157289.1:n.963+960A=
NM_001360.2:c.963+960A= , LRG_340t1:c.963+960A= NP_001351.2:n.963+960A=
XM_011544777.1:c.964-879A= XP_011543079.1:n.964-879A=
XM_011544777.2:c.964-879A= XP_011543079.1:n.964-879A=
NM_001163817.2:c.963+960A= NP_001157289.1:n.963+960A=
NM_001360.3:c.963+960A= MANE Select NP_001351.2:n.963+960A=