Canonical Allele Identifier: CA381694744

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71153309C>G (hg19) ; chr11:g.71442263C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71442263C>G , CM000673.2:g.71442263C>G	GRCh38
NC_000011.9:g.71153309C>G , CM000673.1:g.71153309C>G	GRCh37
NC_000011.8:g.70830957C>G	NCBI36
NG_012655.2:g.11169G>C , LRG_340:g.11169G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.412G>C	ENSP00000435707.3:p.Gly138Arg
ENST00000526780.6:c.412G>C	ENSP00000435668.2:p.Gly138Arg
ENST00000527316.6:c.238G>C	ENSP00000435047.2:p.Gly80Arg
ENST00000682708.1:c.412G>C	ENSP00000506866.1:p.Gly138Arg
ENST00000682880.1:c.412G>C	ENSP00000507520.1:p.Gly138Arg
ENST00000683287.1:c.448G>C	ENSP00000507607.1:p.Gly150Arg
ENST00000683714.1:c.412G>C	ENSP00000508207.1:p.Gly138Arg
ENST00000683874.1:n.689G>C
ENST00000685320.1:c.-174G>C	ENSP00000509319.1:n.-174G>C
ENST00000690257.1:c.316G>C	ENSP00000510750.1:p.Gly106Arg
ENST00000355527.8:c.412G>C MANE Select	ENSP00000347717.4:p.Gly138Arg
ENST00000355527.7:c.412G>C	ENSP00000347717.3:p.Gly138Arg
ENST00000407721.6:c.412G>C	ENSP00000384739.2:p.Gly138Arg
ENST00000526780.5:c.412G>C	ENSP00000435668.1:p.Gly138Arg
ENST00000527316.5:c.316G>C	ENSP00000435047.1:p.Gly106Arg
NM_001163817.1:c.412G>C	NP_001157289.1:p.Gly138Arg
NM_001360.2:c.412G>C , LRG_340t1:c.412G>C	NP_001351.2:p.Gly138Arg
XM_011544777.1:c.412G>C	XP_011543079.1:p.Gly138Arg
XM_011544777.2:c.412G>C	XP_011543079.1:p.Gly138Arg
NM_001163817.2:c.412G>C	NP_001157289.1:p.Gly138Arg
NM_001360.3:c.412G>C MANE Select	NP_001351.2:p.Gly138Arg