Canonical Allele Identifier: CA381703144

Gene: DHCR7

Linked Data

• dbSNP Id: rs1949304698
• MyVariant Identifiers: chr11:g.71148975A>C (hg19) ; chr11:g.71437929A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71437929A>C , CM000673.2:g.71437929A>C	GRCh38
NC_000011.9:g.71148975A>C , CM000673.1:g.71148975A>C	GRCh37
NC_000011.8:g.70826623A>C	NCBI36
NG_012655.2:g.15503T>G , LRG_340:g.15503T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.846T>G	ENSP00000435707.3:p.Ile282Met
ENST00000526780.6:c.846T>G	ENSP00000435668.2:p.Ile282Met
ENST00000527316.6:c.672T>G	ENSP00000435047.2:p.Ile224Met
ENST00000682708.1:c.897T>G	ENSP00000506866.1:p.Ile299Met
ENST00000682880.1:c.846T>G	ENSP00000507520.1:p.Ile282Met
ENST00000683287.1:c.882T>G	ENSP00000507607.1:p.Ile294Met
ENST00000683714.1:c.846T>G	ENSP00000508207.1:p.Ile282Met
ENST00000684396.1:n.886T>G
ENST00000685320.1:c.261T>G	ENSP00000509319.1:p.Ile87Met
ENST00000690257.1:c.750T>G	ENSP00000510750.1:p.Ile250Met
ENST00000355527.8:c.846T>G MANE Select	ENSP00000347717.4:p.Ile282Met
ENST00000355527.7:c.846T>G	ENSP00000347717.3:p.Ile282Met
ENST00000407721.6:c.846T>G	ENSP00000384739.2:p.Ile282Met
ENST00000525137.1:c.213T>G	ENSP00000435956.1:p.Ile71Met
ENST00000527316.5:c.750T>G	ENSP00000435047.1:p.Ile250Met
ENST00000533800.5:c.96T>G	ENSP00000435011.1:p.Ile32Met
ENST00000534795.5:c.202T>G
NM_001163817.1:c.846T>G	NP_001157289.1:p.Ile282Met
NM_001360.2:c.846T>G , LRG_340t1:c.846T>G	NP_001351.2:p.Ile282Met
XM_011544777.1:c.846T>G	XP_011543079.1:p.Ile282Met
XM_011544777.2:c.846T>G	XP_011543079.1:p.Ile282Met
NM_001163817.2:c.846T>G	NP_001157289.1:p.Ile282Met
NM_001360.3:c.846T>G MANE Select	NP_001351.2:p.Ile282Met