Canonical Allele Identifier: CA381703159
Gene: DHCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71437936T>G , CM000673.2:g.71437936T>G GRCh38
NC_000011.9:g.71148982T>G , CM000673.1:g.71148982T>G GRCh37
NC_000011.8:g.70826630T>G NCBI36
NG_012655.2:g.15496A>C , LRG_340:g.15496A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.839A>C ENSP00000435707.3:p.Tyr280Ser
ENST00000526780.6:c.839A>C ENSP00000435668.2:p.Tyr280Ser
ENST00000527316.6:c.665A>C ENSP00000435047.2:p.Tyr222Ser
ENST00000682708.1:c.890A>C ENSP00000506866.1:p.Tyr297Ser
ENST00000682880.1:c.839A>C ENSP00000507520.1:p.Tyr280Ser
ENST00000683287.1:c.875A>C ENSP00000507607.1:p.Tyr292Ser
ENST00000683714.1:c.839A>C ENSP00000508207.1:p.Tyr280Ser
ENST00000684396.1:n.879A>C
ENST00000685320.1:c.254A>C ENSP00000509319.1:p.Tyr85Ser
ENST00000690257.1:c.743A>C ENSP00000510750.1:p.Tyr248Ser
ENST00000355527.8:c.839A>C MANE Select ENSP00000347717.4:p.Tyr280Ser
ENST00000355527.7:c.839A>C ENSP00000347717.3:p.Tyr280Ser
ENST00000407721.6:c.839A>C ENSP00000384739.2:p.Tyr280Ser
ENST00000525137.1:c.206A>C ENSP00000435956.1:p.Tyr69Ser
ENST00000527316.5:c.743A>C ENSP00000435047.1:p.Tyr248Ser
ENST00000533800.5:c.89A>C ENSP00000435011.1:p.Tyr30Ser
ENST00000534795.5:c.195A>C
NM_001163817.1:c.839A>C NP_001157289.1:p.Tyr280Ser
NM_001360.2:c.839A>C , LRG_340t1:c.839A>C NP_001351.2:p.Tyr280Ser
XM_011544777.1:c.839A>C XP_011543079.1:p.Tyr280Ser
XM_011544777.2:c.839A>C XP_011543079.1:p.Tyr280Ser
NM_001163817.2:c.839A>C NP_001157289.1:p.Tyr280Ser
NM_001360.3:c.839A>C MANE Select NP_001351.2:p.Tyr280Ser