Canonical Allele Identifier: CA1981486912
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71435607A= , CM000673.2:g.71435607A= GRCh38
NC_000011.9:g.71146653A= , CM000673.1:g.71146653A= GRCh37
NC_000011.8:g.70824301A= NCBI36
NG_012655.2:g.17825T= , LRG_340:g.17825T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525346.6:c.1196T= ENSP00000435707.3:p.Phe399=
ENST00000526780.6:c.1196T= ENSP00000435668.2:p.Phe399=
ENST00000527316.6:c.1022T= ENSP00000435047.2:p.Phe341=
ENST00000682708.1:c.1247T= ENSP00000506866.1:p.Phe416=
ENST00000683287.1:c.1232T= ENSP00000507607.1:p.Phe411=
ENST00000683714.1:c.1204T= ENSP00000508207.1:p.Ser402=
ENST00000684396.1:n.1236T=
ENST00000685320.1:c.611T= ENSP00000509319.1:p.Phe204=
ENST00000690257.1:c.1100T= ENSP00000510750.1:p.Phe367=
ENST00000355527.8:c.1196T= MANE Select ENSP00000347717.4:p.Phe399=
ENST00000355527.7:c.1196T= ENSP00000347717.3:p.Phe399=
ENST00000407721.6:c.1196T= ENSP00000384739.2:p.Phe399=
ENST00000525137.1:c.697T= ENSP00000435956.1:p.Ser233=
ENST00000533800.5:c.446T= ENSP00000435011.1:p.Phe149=
ENST00000534795.5:c.319+2205T=
NM_001163817.1:c.1196T= NP_001157289.1:p.Phe399=
NM_001360.2:c.1196T= , LRG_340t1:c.1196T= NP_001351.2:p.Phe399=
XM_011544777.1:c.1330T= XP_011543079.1:p.Ser444=
XM_011544777.2:c.1330T= XP_011543079.1:p.Ser444=
NM_001163817.2:c.1196T= NP_001157289.1:p.Phe399=
NM_001360.3:c.1196T= MANE Select NP_001351.2:p.Phe399=