Canonical Allele Identifier: CA381700751

Gene: DHCR7

Linked Data

• dbSNP Id: rs1427783663
• gnomAD v2: 11-71146510-C-G
• gnomAD v4: 11-71435464-C-G
• MyVariant Identifiers: chr11:g.71146510C>G (hg19) ; chr11:g.71435464C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435464C>G , CM000673.2:g.71435464C>G	GRCh38
NC_000011.9:g.71146510C>G , CM000673.1:g.71146510C>G	GRCh37
NC_000011.8:g.70824158C>G	NCBI36
NG_012655.2:g.17968G>C , LRG_340:g.17968G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1339G>C	ENSP00000435707.3:p.Asp447His
ENST00000526780.6:c.1339G>C	ENSP00000435668.2:p.Asp447His
ENST00000527316.6:c.1165G>C	ENSP00000435047.2:p.Asp389His
ENST00000682708.1:c.1390G>C	ENSP00000506866.1:p.Asp464His
ENST00000683287.1:c.1375G>C	ENSP00000507607.1:p.Asp459His
ENST00000683714.1:c.*102G>C	ENSP00000508207.1:n.*102G>C
ENST00000684396.1:n.1379G>C
ENST00000685320.1:c.754G>C	ENSP00000509319.1:p.Asp252His
ENST00000690257.1:c.1243G>C	ENSP00000510750.1:p.Asp415His
ENST00000355527.8:c.1339G>C MANE Select	ENSP00000347717.4:p.Asp447His
ENST00000355527.7:c.1339G>C	ENSP00000347717.3:p.Asp447His
ENST00000407721.6:c.1339G>C	ENSP00000384739.2:p.Asp447His
ENST00000525137.1:c.840G>C	ENSP00000435956.1:n.840G>C
ENST00000533800.5:c.589G>C	ENSP00000435011.1:p.Asp197His
ENST00000534795.5:c.319+2348G>C
NM_001163817.1:c.1339G>C	NP_001157289.1:p.Asp447His
NM_001360.2:c.1339G>C , LRG_340t1:c.1339G>C	NP_001351.2:p.Asp447His
XM_011544777.1:c.*102G>C	XP_011543079.1:n.*102G>C
XM_011544777.2:c.*102G>C	XP_011543079.1:n.*102G>C
NM_001163817.2:c.1339G>C	NP_001157289.1:p.Asp447His
NM_001360.3:c.1339G>C MANE Select	NP_001351.2:p.Asp447His