Canonical Allele Identifier: CA381701982

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146733G>A (hg19) ; chr11:g.71435687G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435687G>A , CM000673.2:g.71435687G>A	GRCh38
NC_000011.9:g.71146733G>A , CM000673.1:g.71146733G>A	GRCh37
NC_000011.8:g.70824381G>A	NCBI36
NG_012655.2:g.17745C>T , LRG_340:g.17745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1116C>T	ENSP00000435707.3:p.Gly372=
ENST00000526780.6:c.1116C>T	ENSP00000435668.2:p.Gly372=
ENST00000527316.6:c.942C>T	ENSP00000435047.2:p.Gly314=
ENST00000682708.1:c.1167C>T	ENSP00000506866.1:p.Gly389=
ENST00000683287.1:c.1152C>T	ENSP00000507607.1:p.Gly384=
ENST00000683714.1:c.1124C>T	ENSP00000508207.1:p.Ala375Val
ENST00000684396.1:n.1156C>T
ENST00000685320.1:c.531C>T	ENSP00000509319.1:p.Gly177=
ENST00000690257.1:c.1020C>T	ENSP00000510750.1:p.Gly340=
ENST00000355527.8:c.1116C>T MANE Select	ENSP00000347717.4:p.Gly372=
ENST00000355527.7:c.1116C>T	ENSP00000347717.3:p.Gly372=
ENST00000407721.6:c.1116C>T	ENSP00000384739.2:p.Gly372=
ENST00000525137.1:c.617C>T	ENSP00000435956.1:p.Ala206Val
ENST00000533800.5:c.366C>T	ENSP00000435011.1:p.Gly122=
ENST00000534795.5:c.319+2125C>T
NM_001163817.1:c.1116C>T	NP_001157289.1:p.Gly372=
NM_001360.2:c.1116C>T , LRG_340t1:c.1116C>T	NP_001351.2:p.Gly372=
XM_011544777.1:c.1250C>T	XP_011543079.1:p.Ala417Val
XM_011544777.2:c.1250C>T	XP_011543079.1:p.Ala417Val
NM_001163817.2:c.1116C>T	NP_001157289.1:p.Gly372=
NM_001360.3:c.1116C>T MANE Select	NP_001351.2:p.Gly372=