Canonical Allele Identifier: CA381700955

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146544G>T (hg19) ; chr11:g.71435498G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435498G>T , CM000673.2:g.71435498G>T	GRCh38
NC_000011.9:g.71146544G>T , CM000673.1:g.71146544G>T	GRCh37
NC_000011.8:g.70824192G>T	NCBI36
NG_012655.2:g.17934C>A , LRG_340:g.17934C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1305C>A	ENSP00000435707.3:p.Tyr435Ter
ENST00000526780.6:c.1305C>A	ENSP00000435668.2:p.Tyr435Ter
ENST00000527316.6:c.1131C>A	ENSP00000435047.2:p.Tyr377Ter
ENST00000682708.1:c.1356C>A	ENSP00000506866.1:p.Tyr452Ter
ENST00000683287.1:c.1341C>A	ENSP00000507607.1:p.Tyr447Ter
ENST00000683714.1:c.*68C>A	ENSP00000508207.1:n.*68C>A
ENST00000684396.1:n.1345C>A
ENST00000685320.1:c.720C>A	ENSP00000509319.1:p.Tyr240Ter
ENST00000690257.1:c.1209C>A	ENSP00000510750.1:p.Tyr403Ter
ENST00000355527.8:c.1305C>A MANE Select	ENSP00000347717.4:p.Tyr435Ter
ENST00000355527.7:c.1305C>A	ENSP00000347717.3:p.Tyr435Ter
ENST00000407721.6:c.1305C>A	ENSP00000384739.2:p.Tyr435Ter
ENST00000525137.1:c.806C>A	ENSP00000435956.1:n.806C>A
ENST00000533800.5:c.555C>A	ENSP00000435011.1:p.Tyr185Ter
ENST00000534795.5:c.319+2314C>A
NM_001163817.1:c.1305C>A	NP_001157289.1:p.Tyr435Ter
NM_001360.2:c.1305C>A , LRG_340t1:c.1305C>A	NP_001351.2:p.Tyr435Ter
XM_011544777.1:c.*68C>A	XP_011543079.1:n.*68C>A
XM_011544777.2:c.*68C>A	XP_011543079.1:n.*68C>A
NM_001163817.2:c.1305C>A	NP_001157289.1:p.Tyr435Ter
NM_001360.3:c.1305C>A MANE Select	NP_001351.2:p.Tyr435Ter