Canonical Allele Identifier: CA2614863371

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71444144-AAGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71444150_71444152del , CM000673.2:g.71444150_71444152del	GRCh38
NC_000011.9:g.71155196_71155198del , CM000673.1:g.71155196_71155198del	GRCh37
NC_000011.8:g.70832844_70832846del	NCBI36
NG_012655.2:g.9285_9287del , LRG_340:g.9285_9287del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.167_169del	ENSP00000435707.3:p.Tyr56del
ENST00000526780.6:c.167_169del	ENSP00000435668.2:p.Tyr56del
ENST00000527316.6:c.-8_-6del	ENSP00000435047.2:n.-8_-6del
ENST00000529990.6:c.-8_-6del	ENSP00000435058.2:n.-8_-6del
ENST00000682708.1:c.167_169del	ENSP00000506866.1:p.Tyr56del
ENST00000682880.1:c.167_169del	ENSP00000507520.1:p.Tyr56del
ENST00000683287.1:c.167_169del	ENSP00000507607.1:p.Tyr56del
ENST00000683714.1:c.167_169del	ENSP00000508207.1:p.Tyr56del
ENST00000683874.1:n.444_446del
ENST00000685320.1:c.-333-86_-333-84del	ENSP00000509319.1:n.-333-86_-333-84del
ENST00000690257.1:c.99-28_99-26del	ENSP00000510750.1:n.99-28_99-26del
ENST00000355527.8:c.167_169del MANE Select	ENSP00000347717.4:p.Tyr56del
ENST00000355527.7:c.167_169del	ENSP00000347717.3:p.Tyr56del
ENST00000407721.6:c.167_169del	ENSP00000384739.2:p.Tyr56del
ENST00000525346.5:c.167_169del	ENSP00000435707.2:p.Tyr56del
ENST00000526780.5:c.167_169del	ENSP00000435668.1:p.Tyr56del
ENST00000527316.5:c.99-28_99-26del	ENSP00000435047.1:n.99-28_99-26del
ENST00000527452.1:c.167_169del	ENSP00000436007.1:p.Tyr56del
ENST00000529990.5:c.107_109del	ENSP00000435058.1:p.Tyr36del
ENST00000531364.5:c.167_169del	ENSP00000432589.1:p.Tyr56del
NM_001163817.1:c.167_169del	NP_001157289.1:p.Tyr56del
NM_001360.2:c.167_169del , LRG_340t1:c.167_169del	NP_001351.2:p.Tyr56del
XM_011544777.1:c.167_169del	XP_011543079.1:p.Tyr56del
XM_011544777.2:c.167_169del	XP_011543079.1:p.Tyr56del
NM_001163817.2:c.167_169del	NP_001157289.1:p.Tyr56del
NM_001360.3:c.167_169del MANE Select	NP_001351.2:p.Tyr56del