Canonical Allele Identifier: CA939372715

Gene: DHCR7

Linked Data

• dbSNP Id: rs1949285851
• gnomAD v3: 11-71436738-T-C
• gnomAD v4: 11-71436738-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71436738T>C , CM000673.2:g.71436738T>C	GRCh38
NC_000011.9:g.71147784T>C , CM000673.1:g.71147784T>C	GRCh37
NC_000011.8:g.70825432T>C	NCBI36
NG_012655.2:g.16694A>G , LRG_340:g.16694A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.964-899A>G	ENSP00000435707.3:n.964-899A>G
ENST00000526780.6:c.964-899A>G	ENSP00000435668.2:n.964-899A>G
ENST00000527316.6:c.790-899A>G	ENSP00000435047.2:n.790-899A>G
ENST00000682708.1:c.1015-899A>G	ENSP00000506866.1:n.1015-899A>G
ENST00000682880.1:c.*936A>G	ENSP00000507520.1:n.*936A>G
ENST00000683287.1:c.1000-899A>G	ENSP00000507607.1:n.1000-899A>G
ENST00000683714.1:c.972-899A>G	ENSP00000508207.1:n.972-899A>G
ENST00000684396.1:n.1004-899A>G
ENST00000685320.1:c.379-899A>G	ENSP00000509319.1:n.379-899A>G
ENST00000690257.1:c.868-899A>G	ENSP00000510750.1:n.868-899A>G
ENST00000355527.8:c.964-899A>G MANE Select	ENSP00000347717.4:n.964-899A>G
ENST00000355527.7:c.964-899A>G	ENSP00000347717.3:n.964-899A>G
ENST00000407721.6:c.964-899A>G	ENSP00000384739.2:n.964-899A>G
ENST00000525137.1:c.331-765A>G	ENSP00000435956.1:n.331-765A>G
ENST00000533800.5:c.214-899A>G	ENSP00000435011.1:n.214-899A>G
ENST00000534795.5:c.319+1074A>G
NM_001163817.1:c.964-899A>G	NP_001157289.1:n.964-899A>G
NM_001360.2:c.964-899A>G , LRG_340t1:c.964-899A>G	NP_001351.2:n.964-899A>G
XM_011544777.1:c.964-765A>G	XP_011543079.1:n.964-765A>G
XM_011544777.2:c.964-765A>G	XP_011543079.1:n.964-765A>G
NM_001163817.2:c.964-899A>G	NP_001157289.1:n.964-899A>G
NM_001360.3:c.964-899A>G MANE Select	NP_001351.2:n.964-899A>G