Canonical Allele Identifier: CA6162255

Gene: DHCR7

Linked Data

• dbSNP Id: rs758040709
• ExAC: 11:71146504 G / A
• gnomAD v2: 11-71146504-G-A
• MyVariant Identifiers: chr11:g.71146504G>A (hg19) ; chr11:g.71435458G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435458G>A , CM000673.2:g.71435458G>A	GRCh38
NC_000011.9:g.71146504G>A , CM000673.1:g.71146504G>A	GRCh37
NC_000011.8:g.70824152G>A	NCBI36
NG_012655.2:g.17974C>T , LRG_340:g.17974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1345C>T	ENSP00000435707.3:p.His449Tyr
ENST00000526780.6:c.1345C>T	ENSP00000435668.2:p.His449Tyr
ENST00000527316.6:c.1171C>T	ENSP00000435047.2:p.His391Tyr
ENST00000682708.1:c.1396C>T	ENSP00000506866.1:p.His466Tyr
ENST00000683287.1:c.1381C>T	ENSP00000507607.1:p.His461Tyr
ENST00000683714.1:c.*108C>T	ENSP00000508207.1:n.*108C>T
ENST00000684396.1:n.1385C>T
ENST00000685320.1:c.760C>T	ENSP00000509319.1:p.His254Tyr
ENST00000690257.1:c.1249C>T	ENSP00000510750.1:p.His417Tyr
ENST00000355527.8:c.1345C>T MANE Select	ENSP00000347717.4:p.His449Tyr
ENST00000355527.7:c.1345C>T	ENSP00000347717.3:p.His449Tyr
ENST00000407721.6:c.1345C>T	ENSP00000384739.2:p.His449Tyr
ENST00000525137.1:c.846C>T	ENSP00000435956.1:n.846C>T
ENST00000533800.5:c.595C>T	ENSP00000435011.1:p.His199Tyr
ENST00000534795.5:c.319+2354C>T
NM_001163817.1:c.1345C>T	NP_001157289.1:p.His449Tyr
NM_001360.2:c.1345C>T , LRG_340t1:c.1345C>T	NP_001351.2:p.His449Tyr
XM_011544777.1:c.*108C>T	XP_011543079.1:n.*108C>T
XM_011544777.2:c.*108C>T	XP_011543079.1:n.*108C>T
NM_001163817.2:c.1345C>T	NP_001157289.1:p.His449Tyr
NM_001360.3:c.1345C>T MANE Select	NP_001351.2:p.His449Tyr