Canonical Allele Identifier: CA381701642

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146671T>G (hg19) ; chr11:g.71435625T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435625T>G , CM000673.2:g.71435625T>G	GRCh38
NC_000011.9:g.71146671T>G , CM000673.1:g.71146671T>G	GRCh37
NC_000011.8:g.70824319T>G	NCBI36
NG_012655.2:g.17807A>C , LRG_340:g.17807A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1178A>C	ENSP00000435707.3:p.Lys393Thr
ENST00000526780.6:c.1178A>C	ENSP00000435668.2:p.Lys393Thr
ENST00000527316.6:c.1004A>C	ENSP00000435047.2:p.Lys335Thr
ENST00000682708.1:c.1229A>C	ENSP00000506866.1:p.Lys410Thr
ENST00000683287.1:c.1214A>C	ENSP00000507607.1:p.Lys405Thr
ENST00000683714.1:c.1186A>C	ENSP00000508207.1:p.Ser396Arg
ENST00000684396.1:n.1218A>C
ENST00000685320.1:c.593A>C	ENSP00000509319.1:p.Lys198Thr
ENST00000690257.1:c.1082A>C	ENSP00000510750.1:p.Lys361Thr
ENST00000355527.8:c.1178A>C MANE Select	ENSP00000347717.4:p.Lys393Thr
ENST00000355527.7:c.1178A>C	ENSP00000347717.3:p.Lys393Thr
ENST00000407721.6:c.1178A>C	ENSP00000384739.2:p.Lys393Thr
ENST00000525137.1:c.679A>C	ENSP00000435956.1:p.Ser227Arg
ENST00000533800.5:c.428A>C	ENSP00000435011.1:p.Lys143Thr
ENST00000534795.5:c.319+2187A>C
NM_001163817.1:c.1178A>C	NP_001157289.1:p.Lys393Thr
NM_001360.2:c.1178A>C , LRG_340t1:c.1178A>C	NP_001351.2:p.Lys393Thr
XM_011544777.1:c.1312A>C	XP_011543079.1:p.Ser438Arg
XM_011544777.2:c.1312A>C	XP_011543079.1:p.Ser438Arg
NM_001163817.2:c.1178A>C	NP_001157289.1:p.Lys393Thr
NM_001360.3:c.1178A>C MANE Select	NP_001351.2:p.Lys393Thr