Canonical Allele Identifier: CA381694552
Community Standard Title: NM_001360.3(DHCR7):c.500G>A (p.Trp167Ter)
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71441353C>T , CM000673.2:g.71441353C>T GRCh38
NC_000011.9:g.71152399C>T , CM000673.1:g.71152399C>T GRCh37
NC_000011.8:g.70830047C>T NCBI36
NG_012655.2:g.12079G>A , LRG_340:g.12079G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001360.3:c.500G>A MANE Select NP_001351.2:p.Trp167Ter
ENST00000355527.8:c.500G>A MANE Select ENSP00000347717.4:p.Trp167Ter
NM_001163817.1:c.500G>A NP_001157289.1:p.Trp167Ter
NM_001163817.2:c.500G>A NP_001157289.1:p.Trp167Ter
NM_001360.2:c.500G>A , LRG_340t1:c.500G>A NP_001351.2:p.Trp167Ter
ENST00000355527.7:c.500G>A ENSP00000347717.3:p.Trp167Ter
ENST00000407721.6:c.500G>A ENSP00000384739.2:p.Trp167Ter
ENST00000525346.6:c.500G>A ENSP00000435707.3:p.Trp167Ter
ENST00000526780.6:c.500G>A ENSP00000435668.2:p.Trp167Ter
ENST00000527316.5:c.404G>A ENSP00000435047.1:p.Trp135Ter
ENST00000527316.6:c.326G>A ENSP00000435047.2:p.Trp109Ter
ENST00000682708.1:c.500G>A ENSP00000506866.1:p.Trp167Ter
ENST00000682880.1:c.500G>A ENSP00000507520.1:p.Trp167Ter
ENST00000683287.1:c.536G>A ENSP00000507607.1:p.Trp179Ter
ENST00000683714.1:c.500G>A ENSP00000508207.1:p.Trp167Ter
ENST00000683874.1:n.777G>A
ENST00000685320.1:c.-86G>A ENSP00000509319.1:n.-86G>A
ENST00000690257.1:c.404G>A ENSP00000510750.1:p.Trp135Ter
XM_011544777.1:c.500G>A XP_011543079.1:p.Trp167Ter
XM_011544777.2:c.500G>A XP_011543079.1:p.Trp167Ter