Canonical Allele Identifier: CA1981486914

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435612C= , CM000673.2:g.71435612C=	GRCh38
NC_000011.9:g.71146658C= , CM000673.1:g.71146658C=	GRCh37
NC_000011.8:g.70824306C=	NCBI36
NG_012655.2:g.17820G= , LRG_340:g.17820G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1191G=	ENSP00000435707.3:p.Ser397=
ENST00000526780.6:c.1191G=	ENSP00000435668.2:p.Ser397=
ENST00000527316.6:c.1017G=	ENSP00000435047.2:p.Ser339=
ENST00000682708.1:c.1242G=	ENSP00000506866.1:p.Ser414=
ENST00000683287.1:c.1227G=	ENSP00000507607.1:p.Ser409=
ENST00000683714.1:c.1199G=	ENSP00000508207.1:p.Arg400=
ENST00000684396.1:n.1231G=
ENST00000685320.1:c.606G=	ENSP00000509319.1:p.Ser202=
ENST00000690257.1:c.1095G=	ENSP00000510750.1:p.Ser365=
ENST00000355527.8:c.1191G= MANE Select	ENSP00000347717.4:p.Ser397=
ENST00000355527.7:c.1191G=	ENSP00000347717.3:p.Ser397=
ENST00000407721.6:c.1191G=	ENSP00000384739.2:p.Ser397=
ENST00000525137.1:c.692G=	ENSP00000435956.1:p.Arg231=
ENST00000533800.5:c.441G=	ENSP00000435011.1:p.Ser147=
ENST00000534795.5:c.319+2200G=
NM_001163817.1:c.1191G=	NP_001157289.1:p.Ser397=
NM_001360.2:c.1191G= , LRG_340t1:c.1191G=	NP_001351.2:p.Ser397=
XM_011544777.1:c.1325G=	XP_011543079.1:p.Arg442=
XM_011544777.2:c.1325G=	XP_011543079.1:p.Arg442=
NM_001163817.2:c.1191G=	NP_001157289.1:p.Ser397=
NM_001360.3:c.1191G= MANE Select	NP_001351.2:p.Ser397=