Canonical Allele Identifier: CA381701945

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71435681-C-A
• MyVariant Identifiers: chr11:g.71146727C>A (hg19) ; chr11:g.71435681C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435681C>A , CM000673.2:g.71435681C>A	GRCh38
NC_000011.9:g.71146727C>A , CM000673.1:g.71146727C>A	GRCh37
NC_000011.8:g.70824375C>A	NCBI36
NG_012655.2:g.17751G>T , LRG_340:g.17751G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1122G>T	ENSP00000435707.3:p.Lys374Asn
ENST00000526780.6:c.1122G>T	ENSP00000435668.2:p.Lys374Asn
ENST00000527316.6:c.948G>T	ENSP00000435047.2:p.Lys316Asn
ENST00000682708.1:c.1173G>T	ENSP00000506866.1:p.Lys391Asn
ENST00000683287.1:c.1158G>T	ENSP00000507607.1:p.Lys386Asn
ENST00000683714.1:c.1130G>T	ENSP00000508207.1:p.Ser377Ile
ENST00000684396.1:n.1162G>T
ENST00000685320.1:c.537G>T	ENSP00000509319.1:p.Lys179Asn
ENST00000690257.1:c.1026G>T	ENSP00000510750.1:p.Lys342Asn
ENST00000355527.8:c.1122G>T MANE Select	ENSP00000347717.4:p.Lys374Asn
ENST00000355527.7:c.1122G>T	ENSP00000347717.3:p.Lys374Asn
ENST00000407721.6:c.1122G>T	ENSP00000384739.2:p.Lys374Asn
ENST00000525137.1:c.623G>T	ENSP00000435956.1:p.Ser208Ile
ENST00000533800.5:c.372G>T	ENSP00000435011.1:p.Lys124Asn
ENST00000534795.5:c.319+2131G>T
NM_001163817.1:c.1122G>T	NP_001157289.1:p.Lys374Asn
NM_001360.2:c.1122G>T , LRG_340t1:c.1122G>T	NP_001351.2:p.Lys374Asn
XM_011544777.1:c.1256G>T	XP_011543079.1:p.Ser419Ile
XM_011544777.2:c.1256G>T	XP_011543079.1:p.Ser419Ile
NM_001163817.2:c.1122G>T	NP_001157289.1:p.Lys374Asn
NM_001360.3:c.1122G>T MANE Select	NP_001351.2:p.Lys374Asn