Canonical Allele Identifier: CA2614856532
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71434649G>A , CM000673.2:g.71434649G>A GRCh38
NC_000011.9:g.71145695G>A , CM000673.1:g.71145695G>A GRCh37
NC_000011.8:g.70823343G>A NCBI36
NG_012655.2:g.18783C>T , LRG_340:g.18783C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.*726C>T ENSP00000435707.3:n.*726C>T
ENST00000526780.6:c.*726C>T ENSP00000435668.2:n.*726C>T
ENST00000682708.1:c.*726C>T ENSP00000506866.1:n.*726C>T
ENST00000683287.1:c.*726C>T ENSP00000507607.1:n.*726C>T
ENST00000683714.1:c.*917C>T ENSP00000508207.1:n.*917C>T
ENST00000684396.1:n.2194C>T
ENST00000685320.1:c.*726C>T ENSP00000509319.1:n.*726C>T
ENST00000690257.1:c.*726C>T ENSP00000510750.1:n.*726C>T
ENST00000355527.8:c.*726C>T MANE Select ENSP00000347717.4:n.*726C>T
ENST00000355527.7:c.*726C>T ENSP00000347717.3:n.*726C>T
ENST00000407721.6:c.*726C>T ENSP00000384739.2:n.*726C>T
ENST00000534795.5:c.319+3163C>T
NM_001163817.1:c.*726C>T NP_001157289.1:n.*726C>T
NM_001360.2:c.*726C>T , LRG_340t1:c.*726C>T NP_001351.2:n.*726C>T
XM_011544777.1:c.*917C>T XP_011543079.1:n.*917C>T
XM_011544777.2:c.*917C>T XP_011543079.1:n.*917C>T
NM_001163817.2:c.*726C>T NP_001157289.1:n.*726C>T
NM_001360.3:c.*726C>T MANE Select NP_001351.2:n.*726C>T