Canonical Allele Identifier: CA381702433

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146836A>G (hg19) ; chr11:g.71435790A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435790A>G , CM000673.2:g.71435790A>G	GRCh38
NC_000011.9:g.71146836A>G , CM000673.1:g.71146836A>G	GRCh37
NC_000011.8:g.70824484A>G	NCBI36
NG_012655.2:g.17642T>C , LRG_340:g.17642T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1013T>C	ENSP00000435707.3:p.Val338Ala
ENST00000526780.6:c.1013T>C	ENSP00000435668.2:p.Val338Ala
ENST00000527316.6:c.839T>C	ENSP00000435047.2:p.Val280Ala
ENST00000682708.1:c.1064T>C	ENSP00000506866.1:p.Val355Ala
ENST00000683287.1:c.1049T>C	ENSP00000507607.1:p.Val350Ala
ENST00000683714.1:c.1021T>C	ENSP00000508207.1:p.Trp341Arg
ENST00000684396.1:n.1053T>C
ENST00000685320.1:c.428T>C	ENSP00000509319.1:p.Val143Ala
ENST00000690257.1:c.917T>C	ENSP00000510750.1:p.Val306Ala
ENST00000355527.8:c.1013T>C MANE Select	ENSP00000347717.4:p.Val338Ala
ENST00000355527.7:c.1013T>C	ENSP00000347717.3:p.Val338Ala
ENST00000407721.6:c.1013T>C	ENSP00000384739.2:p.Val338Ala
ENST00000525137.1:c.514T>C	ENSP00000435956.1:p.Trp172Arg
ENST00000533800.5:c.263T>C	ENSP00000435011.1:p.Val88Ala
ENST00000534795.5:c.319+2022T>C
NM_001163817.1:c.1013T>C	NP_001157289.1:p.Val338Ala
NM_001360.2:c.1013T>C , LRG_340t1:c.1013T>C	NP_001351.2:p.Val338Ala
XM_011544777.1:c.1147T>C	XP_011543079.1:p.Trp383Arg
XM_011544777.2:c.1147T>C	XP_011543079.1:p.Trp383Arg
NM_001163817.2:c.1013T>C	NP_001157289.1:p.Val338Ala
NM_001360.3:c.1013T>C MANE Select	NP_001351.2:p.Val338Ala