Canonical Allele Identifier: CA381703096

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71148956T>A (hg19) ; chr11:g.71437910T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71437910T>A , CM000673.2:g.71437910T>A	GRCh38
NC_000011.9:g.71148956T>A , CM000673.1:g.71148956T>A	GRCh37
NC_000011.8:g.70826604T>A	NCBI36
NG_012655.2:g.15522A>T , LRG_340:g.15522A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.865A>T	ENSP00000435707.3:p.Thr289Ser
ENST00000526780.6:c.865A>T	ENSP00000435668.2:p.Thr289Ser
ENST00000527316.6:c.691A>T	ENSP00000435047.2:p.Thr231Ser
ENST00000682708.1:c.916A>T	ENSP00000506866.1:p.Thr306Ser
ENST00000682880.1:c.865A>T	ENSP00000507520.1:p.Thr289Ser
ENST00000683287.1:c.901A>T	ENSP00000507607.1:p.Thr301Ser
ENST00000683714.1:c.865A>T	ENSP00000508207.1:p.Thr289Ser
ENST00000684396.1:n.905A>T
ENST00000685320.1:c.280A>T	ENSP00000509319.1:p.Thr94Ser
ENST00000690257.1:c.769A>T	ENSP00000510750.1:p.Thr257Ser
ENST00000355527.8:c.865A>T MANE Select	ENSP00000347717.4:p.Thr289Ser
ENST00000355527.7:c.865A>T	ENSP00000347717.3:p.Thr289Ser
ENST00000407721.6:c.865A>T	ENSP00000384739.2:p.Thr289Ser
ENST00000525137.1:c.232A>T	ENSP00000435956.1:p.Thr78Ser
ENST00000527316.5:c.769A>T	ENSP00000435047.1:p.Thr257Ser
ENST00000533800.5:c.115A>T	ENSP00000435011.1:p.Thr39Ser
ENST00000534795.5:c.221A>T
NM_001163817.1:c.865A>T	NP_001157289.1:p.Thr289Ser
NM_001360.2:c.865A>T , LRG_340t1:c.865A>T	NP_001351.2:p.Thr289Ser
XM_011544777.1:c.865A>T	XP_011543079.1:p.Thr289Ser
XM_011544777.2:c.865A>T	XP_011543079.1:p.Thr289Ser
NM_001163817.2:c.865A>T	NP_001157289.1:p.Thr289Ser
NM_001360.3:c.865A>T MANE Select	NP_001351.2:p.Thr289Ser