Canonical Allele Identifier: CA224325615

Gene: DHCR7

Linked Data

• dbSNP Id: rs953793558
• gnomAD v2: 11-71147890-A-G
• gnomAD v3: 11-71436844-A-G
• gnomAD v4: 11-71436844-A-G
• MyVariant Identifiers: chr11:g.71147890A>G (hg19) ; chr11:g.71436844A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71436844A>G , CM000673.2:g.71436844A>G	GRCh38
NC_000011.9:g.71147890A>G , CM000673.1:g.71147890A>G	GRCh37
NC_000011.8:g.70825538A>G	NCBI36
NG_012655.2:g.16588T>C , LRG_340:g.16588T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.963+968T>C	ENSP00000435707.3:n.963+968T>C
ENST00000526780.6:c.963+968T>C	ENSP00000435668.2:n.963+968T>C
ENST00000527316.6:c.789+968T>C	ENSP00000435047.2:n.789+968T>C
ENST00000682708.1:c.1014+968T>C	ENSP00000506866.1:n.1014+968T>C
ENST00000682880.1:c.*830T>C	ENSP00000507520.1:n.*830T>C
ENST00000683287.1:c.999+968T>C	ENSP00000507607.1:n.999+968T>C
ENST00000683714.1:c.971+960T>C	ENSP00000508207.1:n.971+960T>C
ENST00000684396.1:n.1003+968T>C
ENST00000685320.1:c.378+968T>C	ENSP00000509319.1:n.378+968T>C
ENST00000690257.1:c.867+968T>C	ENSP00000510750.1:n.867+968T>C
ENST00000355527.8:c.963+968T>C MANE Select	ENSP00000347717.4:n.963+968T>C
ENST00000355527.7:c.963+968T>C	ENSP00000347717.3:n.963+968T>C
ENST00000407721.6:c.963+968T>C	ENSP00000384739.2:n.963+968T>C
ENST00000525137.1:c.331-871T>C	ENSP00000435956.1:n.331-871T>C
ENST00000533800.5:c.213+968T>C	ENSP00000435011.1:n.213+968T>C
ENST00000534795.5:c.319+968T>C
NM_001163817.1:c.963+968T>C	NP_001157289.1:n.963+968T>C
NM_001360.2:c.963+968T>C , LRG_340t1:c.963+968T>C	NP_001351.2:n.963+968T>C
XM_011544777.1:c.964-871T>C	XP_011543079.1:n.964-871T>C
XM_011544777.2:c.964-871T>C	XP_011543079.1:n.964-871T>C
NM_001163817.2:c.963+968T>C	NP_001157289.1:n.963+968T>C
NM_001360.3:c.963+968T>C MANE Select	NP_001351.2:n.963+968T>C