Canonical Allele Identifier: CA381701106

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146569A>T (hg19) ; chr11:g.71435523A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435523A>T , CM000673.2:g.71435523A>T	GRCh38
NC_000011.9:g.71146569A>T , CM000673.1:g.71146569A>T	GRCh37
NC_000011.8:g.70824217A>T	NCBI36
NG_012655.2:g.17909T>A , LRG_340:g.17909T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.1280T>A	ENSP00000435707.3:p.Leu427Gln
ENST00000526780.6:c.1280T>A	ENSP00000435668.2:p.Leu427Gln
ENST00000527316.6:c.1106T>A	ENSP00000435047.2:p.Leu369Gln
ENST00000682708.1:c.1331T>A	ENSP00000506866.1:p.Leu444Gln
ENST00000683287.1:c.1316T>A	ENSP00000507607.1:p.Leu439Gln
ENST00000683714.1:c.*43T>A	ENSP00000508207.1:n.*43T>A
ENST00000684396.1:n.1320T>A
ENST00000685320.1:c.695T>A	ENSP00000509319.1:p.Leu232Gln
ENST00000690257.1:c.1184T>A	ENSP00000510750.1:p.Leu395Gln
ENST00000355527.8:c.1280T>A MANE Select	ENSP00000347717.4:p.Leu427Gln
ENST00000355527.7:c.1280T>A	ENSP00000347717.3:p.Leu427Gln
ENST00000407721.6:c.1280T>A	ENSP00000384739.2:p.Leu427Gln
ENST00000525137.1:c.781T>A	ENSP00000435956.1:n.781T>A
ENST00000533800.5:c.530T>A	ENSP00000435011.1:p.Leu177Gln
ENST00000534795.5:c.319+2289T>A
NM_001163817.1:c.1280T>A	NP_001157289.1:p.Leu427Gln
NM_001360.2:c.1280T>A , LRG_340t1:c.1280T>A	NP_001351.2:p.Leu427Gln
XM_011544777.1:c.*43T>A	XP_011543079.1:n.*43T>A
XM_011544777.2:c.*43T>A	XP_011543079.1:n.*43T>A
NM_001163817.2:c.1280T>A	NP_001157289.1:p.Leu427Gln
NM_001360.3:c.1280T>A MANE Select	NP_001351.2:p.Leu427Gln