Canonical Allele Identifier: CA381701827

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146704T>G (hg19) ; chr11:g.71435658T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435658T>G , CM000673.2:g.71435658T>G	GRCh38
NC_000011.9:g.71146704T>G , CM000673.1:g.71146704T>G	GRCh37
NC_000011.8:g.70824352T>G	NCBI36
NG_012655.2:g.17774A>C , LRG_340:g.17774A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1145A>C	ENSP00000435707.3:p.Tyr382Ser
ENST00000526780.6:c.1145A>C	ENSP00000435668.2:p.Tyr382Ser
ENST00000527316.6:c.971A>C	ENSP00000435047.2:p.Tyr324Ser
ENST00000682708.1:c.1196A>C	ENSP00000506866.1:p.Tyr399Ser
ENST00000683287.1:c.1181A>C	ENSP00000507607.1:p.Tyr394Ser
ENST00000683714.1:c.1153A>C	ENSP00000508207.1:p.Thr385Pro
ENST00000684396.1:n.1185A>C
ENST00000685320.1:c.560A>C	ENSP00000509319.1:p.Tyr187Ser
ENST00000690257.1:c.1049A>C	ENSP00000510750.1:p.Tyr350Ser
ENST00000355527.8:c.1145A>C MANE Select	ENSP00000347717.4:p.Tyr382Ser
ENST00000355527.7:c.1145A>C	ENSP00000347717.3:p.Tyr382Ser
ENST00000407721.6:c.1145A>C	ENSP00000384739.2:p.Tyr382Ser
ENST00000525137.1:c.646A>C	ENSP00000435956.1:p.Thr216Pro
ENST00000533800.5:c.395A>C	ENSP00000435011.1:p.Tyr132Ser
ENST00000534795.5:c.319+2154A>C
NM_001163817.1:c.1145A>C	NP_001157289.1:p.Tyr382Ser
NM_001360.2:c.1145A>C , LRG_340t1:c.1145A>C	NP_001351.2:p.Tyr382Ser
XM_011544777.1:c.1279A>C	XP_011543079.1:p.Thr427Pro
XM_011544777.2:c.1279A>C	XP_011543079.1:p.Thr427Pro
NM_001163817.2:c.1145A>C	NP_001157289.1:p.Tyr382Ser
NM_001360.3:c.1145A>C MANE Select	NP_001351.2:p.Tyr382Ser