Canonical Allele Identifier: CA381703102
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71437912T>C , CM000673.2:g.71437912T>C GRCh38
NC_000011.9:g.71148958T>C , CM000673.1:g.71148958T>C GRCh37
NC_000011.8:g.70826606T>C NCBI36
NG_012655.2:g.15520A>G , LRG_340:g.15520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.863A>G ENSP00000435707.3:p.Glu288Gly
ENST00000526780.6:c.863A>G ENSP00000435668.2:p.Glu288Gly
ENST00000527316.6:c.689A>G ENSP00000435047.2:p.Glu230Gly
ENST00000682708.1:c.914A>G ENSP00000506866.1:p.Glu305Gly
ENST00000682880.1:c.863A>G ENSP00000507520.1:p.Glu288Gly
ENST00000683287.1:c.899A>G ENSP00000507607.1:p.Glu300Gly
ENST00000683714.1:c.863A>G ENSP00000508207.1:p.Glu288Gly
ENST00000684396.1:n.903A>G
ENST00000685320.1:c.278A>G ENSP00000509319.1:p.Glu93Gly
ENST00000690257.1:c.767A>G ENSP00000510750.1:p.Glu256Gly
ENST00000355527.8:c.863A>G MANE Select ENSP00000347717.4:p.Glu288Gly
ENST00000355527.7:c.863A>G ENSP00000347717.3:p.Glu288Gly
ENST00000407721.6:c.863A>G ENSP00000384739.2:p.Glu288Gly
ENST00000525137.1:c.230A>G ENSP00000435956.1:p.Glu77Gly
ENST00000527316.5:c.767A>G ENSP00000435047.1:p.Glu256Gly
ENST00000533800.5:c.113A>G ENSP00000435011.1:p.Glu38Gly
ENST00000534795.5:c.219A>G
NM_001163817.1:c.863A>G NP_001157289.1:p.Glu288Gly
NM_001360.2:c.863A>G , LRG_340t1:c.863A>G NP_001351.2:p.Glu288Gly
XM_011544777.1:c.863A>G XP_011543079.1:p.Glu288Gly
XM_011544777.2:c.863A>G XP_011543079.1:p.Glu288Gly
NM_001163817.2:c.863A>G NP_001157289.1:p.Glu288Gly
NM_001360.3:c.863A>G MANE Select NP_001351.2:p.Glu288Gly