Canonical Allele Identifier: CA381701784

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146696C>G (hg19) ; chr11:g.71435650C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435650C>G , CM000673.2:g.71435650C>G	GRCh38
NC_000011.9:g.71146696C>G , CM000673.1:g.71146696C>G	GRCh37
NC_000011.8:g.70824344C>G	NCBI36
NG_012655.2:g.17782G>C , LRG_340:g.17782G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1153G>C	ENSP00000435707.3:p.Ala385Pro
ENST00000526780.6:c.1153G>C	ENSP00000435668.2:p.Ala385Pro
ENST00000527316.6:c.979G>C	ENSP00000435047.2:p.Ala327Pro
ENST00000682708.1:c.1204G>C	ENSP00000506866.1:p.Ala402Pro
ENST00000683287.1:c.1189G>C	ENSP00000507607.1:p.Ala397Pro
ENST00000683714.1:c.1161G>C	ENSP00000508207.1:p.Pro387=
ENST00000684396.1:n.1193G>C
ENST00000685320.1:c.568G>C	ENSP00000509319.1:p.Ala190Pro
ENST00000690257.1:c.1057G>C	ENSP00000510750.1:p.Ala353Pro
ENST00000355527.8:c.1153G>C MANE Select	ENSP00000347717.4:p.Ala385Pro
ENST00000355527.7:c.1153G>C	ENSP00000347717.3:p.Ala385Pro
ENST00000407721.6:c.1153G>C	ENSP00000384739.2:p.Ala385Pro
ENST00000525137.1:c.654G>C	ENSP00000435956.1:p.Pro218=
ENST00000533800.5:c.403G>C	ENSP00000435011.1:p.Ala135Pro
ENST00000534795.5:c.319+2162G>C
NM_001163817.1:c.1153G>C	NP_001157289.1:p.Ala385Pro
NM_001360.2:c.1153G>C , LRG_340t1:c.1153G>C	NP_001351.2:p.Ala385Pro
XM_011544777.1:c.1287G>C	XP_011543079.1:p.Pro429=
XM_011544777.2:c.1287G>C	XP_011543079.1:p.Pro429=
NM_001163817.2:c.1153G>C	NP_001157289.1:p.Ala385Pro
NM_001360.3:c.1153G>C MANE Select	NP_001351.2:p.Ala385Pro