Canonical Allele Identifier: CA381701522

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71435601-C-T
• MyVariant Identifiers: chr11:g.71146647C>T (hg19) ; chr11:g.71435601C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435601C>T , CM000673.2:g.71435601C>T	GRCh38
NC_000011.9:g.71146647C>T , CM000673.1:g.71146647C>T	GRCh37
NC_000011.8:g.70824295C>T	NCBI36
NG_012655.2:g.17831G>A , LRG_340:g.17831G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1202G>A	ENSP00000435707.3:p.Gly401Asp
ENST00000526780.6:c.1202G>A	ENSP00000435668.2:p.Gly401Asp
ENST00000527316.6:c.1028G>A	ENSP00000435047.2:p.Gly343Asp
ENST00000682708.1:c.1253G>A	ENSP00000506866.1:p.Gly418Asp
ENST00000683287.1:c.1238G>A	ENSP00000507607.1:p.Gly413Asp
ENST00000683714.1:c.1210G>A	ENSP00000508207.1:p.Ala404Thr
ENST00000684396.1:n.1242G>A
ENST00000685320.1:c.617G>A	ENSP00000509319.1:p.Gly206Asp
ENST00000690257.1:c.1106G>A	ENSP00000510750.1:p.Gly369Asp
ENST00000355527.8:c.1202G>A MANE Select	ENSP00000347717.4:p.Gly401Asp
ENST00000355527.7:c.1202G>A	ENSP00000347717.3:p.Gly401Asp
ENST00000407721.6:c.1202G>A	ENSP00000384739.2:p.Gly401Asp
ENST00000525137.1:c.703G>A	ENSP00000435956.1:p.Ala235Thr
ENST00000533800.5:c.452G>A	ENSP00000435011.1:p.Gly151Asp
ENST00000534795.5:c.319+2211G>A
NM_001163817.1:c.1202G>A	NP_001157289.1:p.Gly401Asp
NM_001360.2:c.1202G>A , LRG_340t1:c.1202G>A	NP_001351.2:p.Gly401Asp
XM_011544777.1:c.1336G>A	XP_011543079.1:p.Ala446Thr
XM_011544777.2:c.1336G>A	XP_011543079.1:p.Ala446Thr
NM_001163817.2:c.1202G>A	NP_001157289.1:p.Gly401Asp
NM_001360.3:c.1202G>A MANE Select	NP_001351.2:p.Gly401Asp