Canonical Allele Identifier: CA6162464
Community Standard Title: NM_001360.3(DHCR7):c.771G>A (p.Ala257=)
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71438939C>T , CM000673.2:g.71438939C>T GRCh38
NC_000011.9:g.71149985C>T , CM000673.1:g.71149985C>T GRCh37
NC_000011.8:g.70827633C>T NCBI36
NG_012655.2:g.14493G>A , LRG_340:g.14493G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001360.3:c.771G>A MANE Select NP_001351.2:p.Ala257=
ENST00000355527.8:c.771G>A MANE Select ENSP00000347717.4:p.Ala257=
NM_001163817.1:c.771G>A NP_001157289.1:p.Ala257=
NM_001163817.2:c.771G>A NP_001157289.1:p.Ala257=
NM_001360.2:c.771G>A , LRG_340t1:c.771G>A NP_001351.2:p.Ala257=
ENST00000355527.7:c.771G>A ENSP00000347717.3:p.Ala257=
ENST00000407721.6:c.771G>A ENSP00000384739.2:p.Ala257=
ENST00000525137.1:c.138G>A ENSP00000435956.1:p.Ala46=
ENST00000525346.6:c.771G>A ENSP00000435707.3:p.Ala257=
ENST00000526780.6:c.771G>A ENSP00000435668.2:p.Ala257=
ENST00000527316.5:c.675G>A ENSP00000435047.1:p.Ala225=
ENST00000527316.6:c.597G>A ENSP00000435047.2:p.Ala199=
ENST00000533800.5:c.21G>A ENSP00000435011.1:p.Ala7=
ENST00000534701.1:n.266G>A
ENST00000534795.5:c.127G>A
ENST00000682708.1:c.822G>A ENSP00000506866.1:p.Ala274=
ENST00000682880.1:c.771G>A ENSP00000507520.1:p.Ala257=
ENST00000683287.1:c.807G>A ENSP00000507607.1:p.Ala269=
ENST00000683714.1:c.771G>A ENSP00000508207.1:p.Ala257=
ENST00000684396.1:n.811G>A
ENST00000685320.1:c.186G>A ENSP00000509319.1:p.Ala62=
ENST00000690257.1:c.675G>A ENSP00000510750.1:p.Ala225=
XM_011544777.1:c.771G>A XP_011543079.1:p.Ala257=
XM_011544777.2:c.771G>A XP_011543079.1:p.Ala257=