Canonical Allele Identifier: CA381701572

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146658C>A (hg19) ; chr11:g.71435612C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1191G>T	ENSP00000435707.3:p.Ser397=
ENST00000526780.6:c.1191G>T	ENSP00000435668.2:p.Ser397=
ENST00000527316.6:c.1017G>T	ENSP00000435047.2:p.Ser339=
ENST00000682708.1:c.1242G>T	ENSP00000506866.1:p.Ser414=
ENST00000683287.1:c.1227G>T	ENSP00000507607.1:p.Ser409=
ENST00000683714.1:c.1199G>T	ENSP00000508207.1:p.Arg400Leu
ENST00000684396.1:n.1231G>T
ENST00000685320.1:c.606G>T	ENSP00000509319.1:p.Ser202=
ENST00000690257.1:c.1095G>T	ENSP00000510750.1:p.Ser365=
ENST00000355527.8:c.1191G>T MANE Select	ENSP00000347717.4:p.Ser397=
ENST00000355527.7:c.1191G>T	ENSP00000347717.3:p.Ser397=
ENST00000407721.6:c.1191G>T	ENSP00000384739.2:p.Ser397=
ENST00000525137.1:c.692G>T	ENSP00000435956.1:p.Arg231Leu
ENST00000533800.5:c.441G>T	ENSP00000435011.1:p.Ser147=
ENST00000534795.5:c.319+2200G>T
NM_001163817.1:c.1191G>T	NP_001157289.1:p.Ser397=
NM_001360.2:c.1191G>T , LRG_340t1:c.1191G>T	NP_001351.2:p.Ser397=
XM_011544777.1:c.1325G>T	XP_011543079.1:p.Arg442Leu
XM_011544777.2:c.1325G>T	XP_011543079.1:p.Arg442Leu
NM_001163817.2:c.1191G>T	NP_001157289.1:p.Ser397=
NM_001360.3:c.1191G>T MANE Select	NP_001351.2:p.Ser397=