Canonical Allele Identifier: CA381702075

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146759T>A (hg19) ; chr11:g.71435713T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435713T>A , CM000673.2:g.71435713T>A	GRCh38
NC_000011.9:g.71146759T>A , CM000673.1:g.71146759T>A	GRCh37
NC_000011.8:g.70824407T>A	NCBI36
NG_012655.2:g.17719A>T , LRG_340:g.17719A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1090A>T	ENSP00000435707.3:p.Thr364Ser
ENST00000526780.6:c.1090A>T	ENSP00000435668.2:p.Thr364Ser
ENST00000527316.6:c.916A>T	ENSP00000435047.2:p.Thr306Ser
ENST00000682708.1:c.1141A>T	ENSP00000506866.1:p.Thr381Ser
ENST00000683287.1:c.1126A>T	ENSP00000507607.1:p.Thr376Ser
ENST00000683714.1:c.1098A>T	ENSP00000508207.1:p.Ala366=
ENST00000684396.1:n.1130A>T
ENST00000685320.1:c.505A>T	ENSP00000509319.1:p.Thr169Ser
ENST00000690257.1:c.994A>T	ENSP00000510750.1:p.Thr332Ser
ENST00000355527.8:c.1090A>T MANE Select	ENSP00000347717.4:p.Thr364Ser
ENST00000355527.7:c.1090A>T	ENSP00000347717.3:p.Thr364Ser
ENST00000407721.6:c.1090A>T	ENSP00000384739.2:p.Thr364Ser
ENST00000525137.1:c.591A>T	ENSP00000435956.1:p.Ala197=
ENST00000533800.5:c.340A>T	ENSP00000435011.1:p.Thr114Ser
ENST00000534795.5:c.319+2099A>T
NM_001163817.1:c.1090A>T	NP_001157289.1:p.Thr364Ser
NM_001360.2:c.1090A>T , LRG_340t1:c.1090A>T	NP_001351.2:p.Thr364Ser
XM_011544777.1:c.1224A>T	XP_011543079.1:p.Ala408=
XM_011544777.2:c.1224A>T	XP_011543079.1:p.Ala408=
NM_001163817.2:c.1090A>T	NP_001157289.1:p.Thr364Ser
NM_001360.3:c.1090A>T MANE Select	NP_001351.2:p.Thr364Ser