Canonical Allele Identifier: CA1981487541
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71436863C= , CM000673.2:g.71436863C= GRCh38
NC_000011.9:g.71147909C= , CM000673.1:g.71147909C= GRCh37
NC_000011.8:g.70825557C= NCBI36
NG_012655.2:g.16569G= , LRG_340:g.16569G=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.963+949G= ENSP00000435707.3:n.963+949G=
ENST00000526780.6:c.963+949G= ENSP00000435668.2:n.963+949G=
ENST00000527316.6:c.789+949G= ENSP00000435047.2:n.789+949G=
ENST00000682708.1:c.1014+949G= ENSP00000506866.1:n.1014+949G=
ENST00000682880.1:c.*811G= ENSP00000507520.1:n.*811G=
ENST00000683287.1:c.999+949G= ENSP00000507607.1:n.999+949G=
ENST00000683714.1:c.971+941G= ENSP00000508207.1:n.971+941G=
ENST00000684396.1:n.1003+949G=
ENST00000685320.1:c.378+949G= ENSP00000509319.1:n.378+949G=
ENST00000690257.1:c.867+949G= ENSP00000510750.1:n.867+949G=
ENST00000355527.8:c.963+949G= MANE Select ENSP00000347717.4:n.963+949G=
ENST00000355527.7:c.963+949G= ENSP00000347717.3:n.963+949G=
ENST00000407721.6:c.963+949G= ENSP00000384739.2:n.963+949G=
ENST00000525137.1:c.331-890G= ENSP00000435956.1:n.331-890G=
ENST00000533800.5:c.213+949G= ENSP00000435011.1:n.213+949G=
ENST00000534795.5:c.319+949G=
NM_001163817.1:c.963+949G= NP_001157289.1:n.963+949G=
NM_001360.2:c.963+949G= , LRG_340t1:c.963+949G= NP_001351.2:n.963+949G=
XM_011544777.1:c.964-890G= XP_011543079.1:n.964-890G=
XM_011544777.2:c.964-890G= XP_011543079.1:n.964-890G=
NM_001163817.2:c.963+949G= NP_001157289.1:n.963+949G=
NM_001360.3:c.963+949G= MANE Select NP_001351.2:n.963+949G=