Canonical Allele Identifier: CA381701809

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146702T>A (hg19) ; chr11:g.71435656T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435656T>A , CM000673.2:g.71435656T>A	GRCh38
NC_000011.9:g.71146702T>A , CM000673.1:g.71146702T>A	GRCh37
NC_000011.8:g.70824350T>A	NCBI36
NG_012655.2:g.17776A>T , LRG_340:g.17776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1147A>T	ENSP00000435707.3:p.Thr383Ser
ENST00000526780.6:c.1147A>T	ENSP00000435668.2:p.Thr383Ser
ENST00000527316.6:c.973A>T	ENSP00000435047.2:p.Thr325Ser
ENST00000682708.1:c.1198A>T	ENSP00000506866.1:p.Thr400Ser
ENST00000683287.1:c.1183A>T	ENSP00000507607.1:p.Thr395Ser
ENST00000683714.1:c.1155A>T	ENSP00000508207.1:p.Thr385=
ENST00000684396.1:n.1187A>T
ENST00000685320.1:c.562A>T	ENSP00000509319.1:p.Thr188Ser
ENST00000690257.1:c.1051A>T	ENSP00000510750.1:p.Thr351Ser
ENST00000355527.8:c.1147A>T MANE Select	ENSP00000347717.4:p.Thr383Ser
ENST00000355527.7:c.1147A>T	ENSP00000347717.3:p.Thr383Ser
ENST00000407721.6:c.1147A>T	ENSP00000384739.2:p.Thr383Ser
ENST00000525137.1:c.648A>T	ENSP00000435956.1:p.Thr216=
ENST00000533800.5:c.397A>T	ENSP00000435011.1:p.Thr133Ser
ENST00000534795.5:c.319+2156A>T
NM_001163817.1:c.1147A>T	NP_001157289.1:p.Thr383Ser
NM_001360.2:c.1147A>T , LRG_340t1:c.1147A>T	NP_001351.2:p.Thr383Ser
XM_011544777.1:c.1281A>T	XP_011543079.1:p.Thr427=
XM_011544777.2:c.1281A>T	XP_011543079.1:p.Thr427=
NM_001163817.2:c.1147A>T	NP_001157289.1:p.Thr383Ser
NM_001360.3:c.1147A>T MANE Select	NP_001351.2:p.Thr383Ser