Canonical Allele Identifier: CA381702179

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146782T>C (hg19) ; chr11:g.71435736T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435736T>C , CM000673.2:g.71435736T>C	GRCh38
NC_000011.9:g.71146782T>C , CM000673.1:g.71146782T>C	GRCh37
NC_000011.8:g.70824430T>C	NCBI36
NG_012655.2:g.17696A>G , LRG_340:g.17696A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1067A>G	ENSP00000435707.3:p.His356Arg
ENST00000526780.6:c.1067A>G	ENSP00000435668.2:p.His356Arg
ENST00000527316.6:c.893A>G	ENSP00000435047.2:p.His298Arg
ENST00000682708.1:c.1118A>G	ENSP00000506866.1:p.His373Arg
ENST00000683287.1:c.1103A>G	ENSP00000507607.1:p.His368Arg
ENST00000683714.1:c.1075A>G	ENSP00000508207.1:p.Thr359Ala
ENST00000684396.1:n.1107A>G
ENST00000685320.1:c.482A>G	ENSP00000509319.1:p.His161Arg
ENST00000690257.1:c.971A>G	ENSP00000510750.1:p.His324Arg
ENST00000355527.8:c.1067A>G MANE Select	ENSP00000347717.4:p.His356Arg
ENST00000355527.7:c.1067A>G	ENSP00000347717.3:p.His356Arg
ENST00000407721.6:c.1067A>G	ENSP00000384739.2:p.His356Arg
ENST00000525137.1:c.568A>G	ENSP00000435956.1:p.Thr190Ala
ENST00000533800.5:c.317A>G	ENSP00000435011.1:p.His106Arg
ENST00000534795.5:c.319+2076A>G
NM_001163817.1:c.1067A>G	NP_001157289.1:p.His356Arg
NM_001360.2:c.1067A>G , LRG_340t1:c.1067A>G	NP_001351.2:p.His356Arg
XM_011544777.1:c.1201A>G	XP_011543079.1:p.Thr401Ala
XM_011544777.2:c.1201A>G	XP_011543079.1:p.Thr401Ala
NM_001163817.2:c.1067A>G	NP_001157289.1:p.His356Arg
NM_001360.3:c.1067A>G MANE Select	NP_001351.2:p.His356Arg