Canonical Allele Identifier: CA381702158
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435731T>G , CM000673.2:g.71435731T>G GRCh38
NC_000011.9:g.71146777T>G , CM000673.1:g.71146777T>G GRCh37
NC_000011.8:g.70824425T>G NCBI36
NG_012655.2:g.17701A>C , LRG_340:g.17701A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.1072A>C ENSP00000435707.3:p.Lys358Gln
ENST00000526780.6:c.1072A>C ENSP00000435668.2:p.Lys358Gln
ENST00000527316.6:c.898A>C ENSP00000435047.2:p.Lys300Gln
ENST00000682708.1:c.1123A>C ENSP00000506866.1:p.Lys375Gln
ENST00000683287.1:c.1108A>C ENSP00000507607.1:p.Lys370Gln
ENST00000683714.1:c.1080A>C ENSP00000508207.1:p.Arg360Ser
ENST00000684396.1:n.1112A>C
ENST00000685320.1:c.487A>C ENSP00000509319.1:p.Lys163Gln
ENST00000690257.1:c.976A>C ENSP00000510750.1:p.Lys326Gln
ENST00000355527.8:c.1072A>C MANE Select ENSP00000347717.4:p.Lys358Gln
ENST00000355527.7:c.1072A>C ENSP00000347717.3:p.Lys358Gln
ENST00000407721.6:c.1072A>C ENSP00000384739.2:p.Lys358Gln
ENST00000525137.1:c.573A>C ENSP00000435956.1:p.Arg191Ser
ENST00000533800.5:c.322A>C ENSP00000435011.1:p.Lys108Gln
ENST00000534795.5:c.319+2081A>C
NM_001163817.1:c.1072A>C NP_001157289.1:p.Lys358Gln
NM_001360.2:c.1072A>C , LRG_340t1:c.1072A>C NP_001351.2:p.Lys358Gln
XM_011544777.1:c.1206A>C XP_011543079.1:p.Arg402Ser
XM_011544777.2:c.1206A>C XP_011543079.1:p.Arg402Ser
NM_001163817.2:c.1072A>C NP_001157289.1:p.Lys358Gln
NM_001360.3:c.1072A>C MANE Select NP_001351.2:p.Lys358Gln