Canonical Allele Identifier: CA381701039

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146558A>C (hg19) ; chr11:g.71435512A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435512A>C , CM000673.2:g.71435512A>C	GRCh38
NC_000011.9:g.71146558A>C , CM000673.1:g.71146558A>C	GRCh37
NC_000011.8:g.70824206A>C	NCBI36
NG_012655.2:g.17920T>G , LRG_340:g.17920T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.1291T>G	ENSP00000435707.3:p.Phe431Val
ENST00000526780.6:c.1291T>G	ENSP00000435668.2:p.Phe431Val
ENST00000527316.6:c.1117T>G	ENSP00000435047.2:p.Phe373Val
ENST00000682708.1:c.1342T>G	ENSP00000506866.1:p.Phe448Val
ENST00000683287.1:c.1327T>G	ENSP00000507607.1:p.Phe443Val
ENST00000683714.1:c.*54T>G	ENSP00000508207.1:n.*54T>G
ENST00000684396.1:n.1331T>G
ENST00000685320.1:c.706T>G	ENSP00000509319.1:p.Phe236Val
ENST00000690257.1:c.1195T>G	ENSP00000510750.1:p.Phe399Val
ENST00000355527.8:c.1291T>G MANE Select	ENSP00000347717.4:p.Phe431Val
ENST00000355527.7:c.1291T>G	ENSP00000347717.3:p.Phe431Val
ENST00000407721.6:c.1291T>G	ENSP00000384739.2:p.Phe431Val
ENST00000525137.1:c.792T>G	ENSP00000435956.1:n.792T>G
ENST00000533800.5:c.541T>G	ENSP00000435011.1:p.Phe181Val
ENST00000534795.5:c.319+2300T>G
NM_001163817.1:c.1291T>G	NP_001157289.1:p.Phe431Val
NM_001360.2:c.1291T>G , LRG_340t1:c.1291T>G	NP_001351.2:p.Phe431Val
XM_011544777.1:c.*54T>G	XP_011543079.1:n.*54T>G
XM_011544777.2:c.*54T>G	XP_011543079.1:n.*54T>G
NM_001163817.2:c.1291T>G	NP_001157289.1:p.Phe431Val
NM_001360.3:c.1291T>G MANE Select	NP_001351.2:p.Phe431Val