Canonical Allele Identifier: CA1981486805

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435427C= , CM000673.2:g.71435427C=	GRCh38
NC_000011.9:g.71146473C= , CM000673.1:g.71146473C=	GRCh37
NC_000011.8:g.70824121C=	NCBI36
NG_012655.2:g.18005G= , LRG_340:g.18005G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1376G=	ENSP00000435707.3:p.Trp459=
ENST00000526780.6:c.1376G=	ENSP00000435668.2:p.Trp459=
ENST00000527316.6:c.1202G=	ENSP00000435047.2:p.Trp401=
ENST00000682708.1:c.1427G=	ENSP00000506866.1:p.Trp476=
ENST00000683287.1:c.1412G=	ENSP00000507607.1:p.Trp471=
ENST00000683714.1:c.*139G=	ENSP00000508207.1:n.*139G=
ENST00000684396.1:n.1416G=
ENST00000685320.1:c.791G=	ENSP00000509319.1:p.Trp264=
ENST00000690257.1:c.1280G=	ENSP00000510750.1:p.Trp427=
ENST00000355527.8:c.1376G= MANE Select	ENSP00000347717.4:p.Trp459=
ENST00000355527.7:c.1376G=	ENSP00000347717.3:p.Trp459=
ENST00000407721.6:c.1376G=	ENSP00000384739.2:p.Trp459=
ENST00000525137.1:c.877G=	ENSP00000435956.1:n.877G=
ENST00000533800.5:c.611+15G=	ENSP00000435011.1:n.611+15G=
ENST00000534795.5:c.319+2385G=
NM_001163817.1:c.1376G=	NP_001157289.1:p.Trp459=
NM_001360.2:c.1376G= , LRG_340t1:c.1376G=	NP_001351.2:p.Trp459=
XM_011544777.1:c.*139G=	XP_011543079.1:n.*139G=
XM_011544777.2:c.*139G=	XP_011543079.1:n.*139G=
NM_001163817.2:c.1376G=	NP_001157289.1:p.Trp459=
NM_001360.3:c.1376G= MANE Select	NP_001351.2:p.Trp459=