Canonical Allele Identifier: CA1981491083
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71444143G= , CM000673.2:g.71444143G= GRCh38
NC_000011.9:g.71155189G= , CM000673.1:g.71155189G= GRCh37
NC_000011.8:g.70832837G= NCBI36
NG_012655.2:g.9289C= , LRG_340:g.9289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.171C= ENSP00000435707.3:p.Phe57=
ENST00000526780.6:c.171C= ENSP00000435668.2:p.Phe57=
ENST00000527316.6:c.-4C= ENSP00000435047.2:n.-4C=
ENST00000529990.6:c.-4C= ENSP00000435058.2:n.-4C=
ENST00000682708.1:c.171C= ENSP00000506866.1:p.Phe57=
ENST00000682880.1:c.171C= ENSP00000507520.1:p.Phe57=
ENST00000683287.1:c.171C= ENSP00000507607.1:p.Phe57=
ENST00000683714.1:c.171C= ENSP00000508207.1:p.Phe57=
ENST00000683874.1:n.448C=
ENST00000685320.1:c.-333-82C= ENSP00000509319.1:n.-333-82C=
ENST00000690257.1:c.99-24C= ENSP00000510750.1:n.99-24C=
ENST00000355527.8:c.171C= MANE Select ENSP00000347717.4:p.Phe57=
ENST00000355527.7:c.171C= ENSP00000347717.3:p.Phe57=
ENST00000407721.6:c.171C= ENSP00000384739.2:p.Phe57=
ENST00000525346.5:c.171C= ENSP00000435707.2:p.Phe57=
ENST00000526780.5:c.171C= ENSP00000435668.1:p.Phe57=
ENST00000527316.5:c.99-24C= ENSP00000435047.1:n.99-24C=
ENST00000527452.1:c.171C= ENSP00000436007.1:p.Phe57=
ENST00000529990.5:c.111C= ENSP00000435058.1:p.Phe37=
ENST00000531364.5:c.171C= ENSP00000432589.1:p.Phe57=
NM_001163817.1:c.171C= NP_001157289.1:p.Phe57=
NM_001360.2:c.171C= , LRG_340t1:c.171C= NP_001351.2:p.Phe57=
XM_011544777.1:c.171C= XP_011543079.1:p.Phe57=
XM_011544777.2:c.171C= XP_011543079.1:p.Phe57=
NM_001163817.2:c.171C= NP_001157289.1:p.Phe57=
NM_001360.3:c.171C= MANE Select NP_001351.2:p.Phe57=