Canonical Allele Identifier: CA6162283
Gene: DHCR7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1121396
dbSNP Id: rs777148033

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435579G>A , CM000673.2:g.71435579G>A GRCh38
NC_000011.9:g.71146625G>A , CM000673.1:g.71146625G>A GRCh37
NC_000011.8:g.70824273G>A NCBI36
NG_012655.2:g.17853C>T , LRG_340:g.17853C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.1224C>T ENSP00000435707.3:p.Tyr408=
ENST00000526780.6:c.1224C>T ENSP00000435668.2:p.Tyr408=
ENST00000527316.6:c.1050C>T ENSP00000435047.2:p.Tyr350=
ENST00000682708.1:c.1275C>T ENSP00000506866.1:p.Tyr425=
ENST00000683287.1:c.1260C>T ENSP00000507607.1:p.Tyr420=
ENST00000683714.1:c.1232C>T ENSP00000508207.1:p.Thr411Met
ENST00000684396.1:n.1264C>T
ENST00000685320.1:c.639C>T ENSP00000509319.1:p.Tyr213=
ENST00000690257.1:c.1128C>T ENSP00000510750.1:p.Tyr376=
ENST00000355527.8:c.1224C>T MANE Select ENSP00000347717.4:p.Tyr408=
ENST00000355527.7:c.1224C>T ENSP00000347717.3:p.Tyr408=
ENST00000407721.6:c.1224C>T ENSP00000384739.2:p.Tyr408=
ENST00000525137.1:c.725C>T ENSP00000435956.1:p.Thr242Met
ENST00000533800.5:c.474C>T ENSP00000435011.1:p.Tyr158=
ENST00000534795.5:c.319+2233C>T
NM_001163817.1:c.1224C>T NP_001157289.1:p.Tyr408=
NM_001360.2:c.1224C>T , LRG_340t1:c.1224C>T NP_001351.2:p.Tyr408=
XM_011544777.1:c.1358C>T XP_011543079.1:p.Thr453Met
XM_011544777.2:c.1358C>T XP_011543079.1:p.Thr453Met
NM_001163817.2:c.1224C>T NP_001157289.1:p.Tyr408=
NM_001360.3:c.1224C>T MANE Select NP_001351.2:p.Tyr408=