Canonical Allele Identifier: CA381701588

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146662A>G (hg19) ; chr11:g.71435616A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435616A>G , CM000673.2:g.71435616A>G	GRCh38
NC_000011.9:g.71146662A>G , CM000673.1:g.71146662A>G	GRCh37
NC_000011.8:g.70824310A>G	NCBI36
NG_012655.2:g.17816T>C , LRG_340:g.17816T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.1187T>C	ENSP00000435707.3:p.Val396Ala
ENST00000526780.6:c.1187T>C	ENSP00000435668.2:p.Val396Ala
ENST00000527316.6:c.1013T>C	ENSP00000435047.2:p.Val338Ala
ENST00000682708.1:c.1238T>C	ENSP00000506866.1:p.Val413Ala
ENST00000683287.1:c.1223T>C	ENSP00000507607.1:p.Val408Ala
ENST00000683714.1:c.1195T>C	ENSP00000508207.1:p.Cys399Arg
ENST00000684396.1:n.1227T>C
ENST00000685320.1:c.602T>C	ENSP00000509319.1:p.Val201Ala
ENST00000690257.1:c.1091T>C	ENSP00000510750.1:p.Val364Ala
ENST00000355527.8:c.1187T>C MANE Select	ENSP00000347717.4:p.Val396Ala
ENST00000355527.7:c.1187T>C	ENSP00000347717.3:p.Val396Ala
ENST00000407721.6:c.1187T>C	ENSP00000384739.2:p.Val396Ala
ENST00000525137.1:c.688T>C	ENSP00000435956.1:p.Cys230Arg
ENST00000533800.5:c.437T>C	ENSP00000435011.1:p.Val146Ala
ENST00000534795.5:c.319+2196T>C
NM_001163817.1:c.1187T>C	NP_001157289.1:p.Val396Ala
NM_001360.2:c.1187T>C , LRG_340t1:c.1187T>C	NP_001351.2:p.Val396Ala
XM_011544777.1:c.1321T>C	XP_011543079.1:p.Cys441Arg
XM_011544777.2:c.1321T>C	XP_011543079.1:p.Cys441Arg
NM_001163817.2:c.1187T>C	NP_001157289.1:p.Val396Ala
NM_001360.3:c.1187T>C MANE Select	NP_001351.2:p.Val396Ala