Canonical Allele Identifier: CA381702884

Gene: DHCR7

Linked Data

• ClinVar Variation Id: 990551
• ClinVar RCV Id: RCV001278596
• dbSNP Id: rs1949301409
• MyVariant Identifiers: chr11:g.71148862A>G (hg19) ; chr11:g.71437816A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71437816A>G , CM000673.2:g.71437816A>G	GRCh38
NC_000011.9:g.71148862A>G , CM000673.1:g.71148862A>G	GRCh37
NC_000011.8:g.70826510A>G	NCBI36
NG_012655.2:g.15616T>C , LRG_340:g.15616T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.959T>C	ENSP00000435707.3:p.Leu320Pro
ENST00000526780.6:c.959T>C	ENSP00000435668.2:p.Leu320Pro
ENST00000527316.6:c.785T>C	ENSP00000435047.2:p.Leu262Pro
ENST00000682708.1:c.1010T>C	ENSP00000506866.1:p.Leu337Pro
ENST00000682880.1:c.959T>C	ENSP00000507520.1:p.Leu320Pro
ENST00000683287.1:c.995T>C	ENSP00000507607.1:p.Leu332Pro
ENST00000683714.1:c.959T>C	ENSP00000508207.1:p.Leu320Pro
ENST00000684396.1:n.999T>C
ENST00000685320.1:c.374T>C	ENSP00000509319.1:p.Leu125Pro
ENST00000690257.1:c.863T>C	ENSP00000510750.1:p.Leu288Pro
ENST00000355527.8:c.959T>C MANE Select	ENSP00000347717.4:p.Leu320Pro
ENST00000355527.7:c.959T>C	ENSP00000347717.3:p.Leu320Pro
ENST00000407721.6:c.959T>C	ENSP00000384739.2:p.Leu320Pro
ENST00000525137.1:c.326T>C	ENSP00000435956.1:p.Leu109Pro
ENST00000533800.5:c.209T>C	ENSP00000435011.1:p.Leu70Pro
ENST00000534795.5:c.315T>C
NM_001163817.1:c.959T>C	NP_001157289.1:p.Leu320Pro
NM_001360.2:c.959T>C , LRG_340t1:c.959T>C	NP_001351.2:p.Leu320Pro
XM_011544777.1:c.959T>C	XP_011543079.1:p.Leu320Pro
XM_011544777.2:c.959T>C	XP_011543079.1:p.Leu320Pro
NM_001163817.2:c.959T>C	NP_001157289.1:p.Leu320Pro
NM_001360.3:c.959T>C MANE Select	NP_001351.2:p.Leu320Pro