Canonical Allele Identifier: CA2614856814

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71434887-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71434887C>A , CM000673.2:g.71434887C>A	GRCh38
NC_000011.9:g.71145933C>A , CM000673.1:g.71145933C>A	GRCh37
NC_000011.8:g.70823581C>A	NCBI36
NG_012655.2:g.18545G>T , LRG_340:g.18545G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.*488G>T	ENSP00000435707.3:n.*488G>T
ENST00000526780.6:c.*488G>T	ENSP00000435668.2:n.*488G>T
ENST00000682708.1:c.*488G>T	ENSP00000506866.1:n.*488G>T
ENST00000683287.1:c.*488G>T	ENSP00000507607.1:n.*488G>T
ENST00000683714.1:c.*679G>T	ENSP00000508207.1:n.*679G>T
ENST00000684396.1:n.1956G>T
ENST00000685320.1:c.*488G>T	ENSP00000509319.1:n.*488G>T
ENST00000690257.1:c.*488G>T	ENSP00000510750.1:n.*488G>T
ENST00000355527.8:c.*488G>T MANE Select	ENSP00000347717.4:n.*488G>T
ENST00000355527.7:c.*488G>T	ENSP00000347717.3:n.*488G>T
ENST00000407721.6:c.*488G>T	ENSP00000384739.2:n.*488G>T
ENST00000534795.5:c.319+2925G>T
NM_001163817.1:c.*488G>T	NP_001157289.1:n.*488G>T
NM_001360.2:c.*488G>T , LRG_340t1:c.*488G>T	NP_001351.2:n.*488G>T
XM_011544777.1:c.*679G>T	XP_011543079.1:n.*679G>T
XM_011544777.2:c.*679G>T	XP_011543079.1:n.*679G>T
NM_001163817.2:c.*488G>T	NP_001157289.1:n.*488G>T
NM_001360.3:c.*488G>T MANE Select	NP_001351.2:n.*488G>T