Canonical Allele Identifier: CA381702121

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146768A>T (hg19) ; chr11:g.71435722A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435722A>T , CM000673.2:g.71435722A>T	GRCh38
NC_000011.9:g.71146768A>T , CM000673.1:g.71146768A>T	GRCh37
NC_000011.8:g.70824416A>T	NCBI36
NG_012655.2:g.17710T>A , LRG_340:g.17710T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1081T>A	ENSP00000435707.3:p.Phe361Ile
ENST00000526780.6:c.1081T>A	ENSP00000435668.2:p.Phe361Ile
ENST00000527316.6:c.907T>A	ENSP00000435047.2:p.Phe303Ile
ENST00000682708.1:c.1132T>A	ENSP00000506866.1:p.Phe378Ile
ENST00000683287.1:c.1117T>A	ENSP00000507607.1:p.Phe373Ile
ENST00000683714.1:c.1089T>A	ENSP00000508207.1:p.Cys363Ter
ENST00000684396.1:n.1121T>A
ENST00000685320.1:c.496T>A	ENSP00000509319.1:p.Phe166Ile
ENST00000690257.1:c.985T>A	ENSP00000510750.1:p.Phe329Ile
ENST00000355527.8:c.1081T>A MANE Select	ENSP00000347717.4:p.Phe361Ile
ENST00000355527.7:c.1081T>A	ENSP00000347717.3:p.Phe361Ile
ENST00000407721.6:c.1081T>A	ENSP00000384739.2:p.Phe361Ile
ENST00000525137.1:c.582T>A	ENSP00000435956.1:p.Cys194Ter
ENST00000533800.5:c.331T>A	ENSP00000435011.1:p.Phe111Ile
ENST00000534795.5:c.319+2090T>A
NM_001163817.1:c.1081T>A	NP_001157289.1:p.Phe361Ile
NM_001360.2:c.1081T>A , LRG_340t1:c.1081T>A	NP_001351.2:p.Phe361Ile
XM_011544777.1:c.1215T>A	XP_011543079.1:p.Cys405Ter
XM_011544777.2:c.1215T>A	XP_011543079.1:p.Cys405Ter
NM_001163817.2:c.1081T>A	NP_001157289.1:p.Phe361Ile
NM_001360.3:c.1081T>A MANE Select	NP_001351.2:p.Phe361Ile