Canonical Allele Identifier: CA381700646
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435443T>G , CM000673.2:g.71435443T>G GRCh38
NC_000011.9:g.71146489T>G , CM000673.1:g.71146489T>G GRCh37
NC_000011.8:g.70824137T>G NCBI36
NG_012655.2:g.17989A>C , LRG_340:g.17989A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.1360A>C ENSP00000435707.3:p.Lys454Gln
ENST00000526780.6:c.1360A>C ENSP00000435668.2:p.Lys454Gln
ENST00000527316.6:c.1186A>C ENSP00000435047.2:p.Lys396Gln
ENST00000682708.1:c.1411A>C ENSP00000506866.1:p.Lys471Gln
ENST00000683287.1:c.1396A>C ENSP00000507607.1:p.Lys466Gln
ENST00000683714.1:c.*123A>C ENSP00000508207.1:n.*123A>C
ENST00000684396.1:n.1400A>C
ENST00000685320.1:c.775A>C ENSP00000509319.1:p.Lys259Gln
ENST00000690257.1:c.1264A>C ENSP00000510750.1:p.Lys422Gln
ENST00000355527.8:c.1360A>C MANE Select ENSP00000347717.4:p.Lys454Gln
ENST00000355527.7:c.1360A>C ENSP00000347717.3:p.Lys454Gln
ENST00000407721.6:c.1360A>C ENSP00000384739.2:p.Lys454Gln
ENST00000525137.1:c.861A>C ENSP00000435956.1:n.861A>C
ENST00000533800.5:c.610A>C ENSP00000435011.1:p.Lys204Gln
ENST00000534795.5:c.319+2369A>C
NM_001163817.1:c.1360A>C NP_001157289.1:p.Lys454Gln
NM_001360.2:c.1360A>C , LRG_340t1:c.1360A>C NP_001351.2:p.Lys454Gln
XM_011544777.1:c.*123A>C XP_011543079.1:n.*123A>C
XM_011544777.2:c.*123A>C XP_011543079.1:n.*123A>C
NM_001163817.2:c.1360A>C NP_001157289.1:p.Lys454Gln
NM_001360.3:c.1360A>C MANE Select NP_001351.2:p.Lys454Gln