Canonical Allele Identifier: CA381696220
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71444043G>T , CM000673.2:g.71444043G>T GRCh38
NC_000011.9:g.71155089G>T , CM000673.1:g.71155089G>T GRCh37
NC_000011.8:g.70832737G>T NCBI36
NG_012655.2:g.9389C>A , LRG_340:g.9389C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.271C>A ENSP00000435707.3:p.Pro91Thr
ENST00000526780.6:c.271C>A ENSP00000435668.2:p.Pro91Thr
ENST00000527316.6:c.97C>A ENSP00000435047.2:p.Pro33Thr
ENST00000529990.6:c.97C>A ENSP00000435058.2:p.Pro33Thr
ENST00000682708.1:c.271C>A ENSP00000506866.1:p.Pro91Thr
ENST00000682880.1:c.271C>A ENSP00000507520.1:p.Pro91Thr
ENST00000683287.1:c.271C>A ENSP00000507607.1:p.Pro91Thr
ENST00000683714.1:c.271C>A ENSP00000508207.1:p.Pro91Thr
ENST00000683874.1:n.548C>A
ENST00000685320.1:c.-315C>A ENSP00000509319.1:n.-315C>A
ENST00000690257.1:c.175C>A ENSP00000510750.1:p.Pro59Thr
ENST00000355527.8:c.271C>A MANE Select ENSP00000347717.4:p.Pro91Thr
ENST00000355527.7:c.271C>A ENSP00000347717.3:p.Pro91Thr
ENST00000407721.6:c.271C>A ENSP00000384739.2:p.Pro91Thr
ENST00000525346.5:c.271C>A ENSP00000435707.2:p.Pro91Thr
ENST00000526780.5:c.271C>A ENSP00000435668.1:p.Pro91Thr
ENST00000527316.5:c.175C>A ENSP00000435047.1:p.Pro59Thr
ENST00000527452.1:c.271C>A ENSP00000436007.1:p.Pro91Thr
ENST00000529990.5:c.211C>A ENSP00000435058.1:p.Pro71Thr
ENST00000531364.5:c.271C>A ENSP00000432589.1:p.Pro91Thr
NM_001163817.1:c.271C>A NP_001157289.1:p.Pro91Thr
NM_001360.2:c.271C>A , LRG_340t1:c.271C>A NP_001351.2:p.Pro91Thr
XM_011544777.1:c.271C>A XP_011543079.1:p.Pro91Thr
XM_011544777.2:c.271C>A XP_011543079.1:p.Pro91Thr
NM_001163817.2:c.271C>A NP_001157289.1:p.Pro91Thr
NM_001360.3:c.271C>A MANE Select NP_001351.2:p.Pro91Thr