Canonical Allele Identifier: CA381701441

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146634G>T (hg19) ; chr11:g.71435588G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435588G>T , CM000673.2:g.71435588G>T	GRCh38
NC_000011.9:g.71146634G>T , CM000673.1:g.71146634G>T	GRCh37
NC_000011.8:g.70824282G>T	NCBI36
NG_012655.2:g.17844C>A , LRG_340:g.17844C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1215C>A	ENSP00000435707.3:p.His405Gln
ENST00000526780.6:c.1215C>A	ENSP00000435668.2:p.His405Gln
ENST00000527316.6:c.1041C>A	ENSP00000435047.2:p.His347Gln
ENST00000682708.1:c.1266C>A	ENSP00000506866.1:p.His422Gln
ENST00000683287.1:c.1251C>A	ENSP00000507607.1:p.His417Gln
ENST00000683714.1:c.1223C>A	ENSP00000508207.1:p.Thr408Asn
ENST00000684396.1:n.1255C>A
ENST00000685320.1:c.630C>A	ENSP00000509319.1:p.His210Gln
ENST00000690257.1:c.1119C>A	ENSP00000510750.1:p.His373Gln
ENST00000355527.8:c.1215C>A MANE Select	ENSP00000347717.4:p.His405Gln
ENST00000355527.7:c.1215C>A	ENSP00000347717.3:p.His405Gln
ENST00000407721.6:c.1215C>A	ENSP00000384739.2:p.His405Gln
ENST00000525137.1:c.716C>A	ENSP00000435956.1:p.Thr239Asn
ENST00000533800.5:c.465C>A	ENSP00000435011.1:p.His155Gln
ENST00000534795.5:c.319+2224C>A
NM_001163817.1:c.1215C>A	NP_001157289.1:p.His405Gln
NM_001360.2:c.1215C>A , LRG_340t1:c.1215C>A	NP_001351.2:p.His405Gln
XM_011544777.1:c.1349C>A	XP_011543079.1:p.Thr450Asn
XM_011544777.2:c.1349C>A	XP_011543079.1:p.Thr450Asn
NM_001163817.2:c.1215C>A	NP_001157289.1:p.His405Gln
NM_001360.3:c.1215C>A MANE Select	NP_001351.2:p.His405Gln