Canonical Allele Identifier: CA6162372

Gene: DHCR7

Linked Data

• dbSNP Id: rs754273826
• ExAC: 11:71146959 AG / A
• MyVariant Identifiers: chr11:g.71146960del (hg19) ; chr11:g.71435914del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435914del , CM000673.2:g.71435914del	GRCh38
NC_000011.9:g.71146960del , CM000673.1:g.71146960del	GRCh37
NC_000011.8:g.70824608del	NCBI36
NG_012655.2:g.17518del , LRG_340:g.17518del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.964-75del	ENSP00000435707.3:n.964-75del
ENST00000526780.6:c.964-75del	ENSP00000435668.2:n.964-75del
ENST00000527316.6:c.790-75del	ENSP00000435047.2:n.790-75del
ENST00000682708.1:c.1015-75del	ENSP00000506866.1:n.1015-75del
ENST00000683287.1:c.1000-75del	ENSP00000507607.1:n.1000-75del
ENST00000683714.1:c.972-75del	ENSP00000508207.1:n.972-75del
ENST00000684396.1:n.1004-75del
ENST00000685320.1:c.379-75del	ENSP00000509319.1:n.379-75del
ENST00000690257.1:c.868-75del	ENSP00000510750.1:n.868-75del
ENST00000355527.8:c.964-75del MANE Select	ENSP00000347717.4:n.964-75del
ENST00000355527.7:c.964-75del	ENSP00000347717.3:n.964-75del
ENST00000407721.6:c.964-75del	ENSP00000384739.2:n.964-75del
ENST00000525137.1:c.390del	ENSP00000435956.1:p.Trp131GlyfsTer17
ENST00000533800.5:c.214-75del	ENSP00000435011.1:n.214-75del
ENST00000534795.5:c.319+1898del
NM_001163817.1:c.964-75del	NP_001157289.1:n.964-75del
NM_001360.2:c.964-75del , LRG_340t1:c.964-75del	NP_001351.2:n.964-75del
XM_011544777.1:c.1023del	XP_011543079.1:p.Trp342GlyfsTer17
XM_011544777.2:c.1023del	XP_011543079.1:p.Trp342GlyfsTer17
NM_001163817.2:c.964-75del	NP_001157289.1:n.964-75del
NM_001360.3:c.964-75del MANE Select	NP_001351.2:n.964-75del