Canonical Allele Identifier: CA381694778

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71153315G>T (hg19) ; chr11:g.71442269G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71442269G>T , CM000673.2:g.71442269G>T	GRCh38
NC_000011.9:g.71153315G>T , CM000673.1:g.71153315G>T	GRCh37
NC_000011.8:g.70830963G>T	NCBI36
NG_012655.2:g.11163C>A , LRG_340:g.11163C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.406C>A	ENSP00000435707.3:p.Pro136Thr
ENST00000526780.6:c.406C>A	ENSP00000435668.2:p.Pro136Thr
ENST00000527316.6:c.232C>A	ENSP00000435047.2:p.Pro78Thr
ENST00000682708.1:c.406C>A	ENSP00000506866.1:p.Pro136Thr
ENST00000682880.1:c.406C>A	ENSP00000507520.1:p.Pro136Thr
ENST00000683287.1:c.442C>A	ENSP00000507607.1:p.Pro148Thr
ENST00000683714.1:c.406C>A	ENSP00000508207.1:p.Pro136Thr
ENST00000683874.1:n.683C>A
ENST00000685320.1:c.-180C>A	ENSP00000509319.1:n.-180C>A
ENST00000690257.1:c.310C>A	ENSP00000510750.1:p.Pro104Thr
ENST00000355527.8:c.406C>A MANE Select	ENSP00000347717.4:p.Pro136Thr
ENST00000355527.7:c.406C>A	ENSP00000347717.3:p.Pro136Thr
ENST00000407721.6:c.406C>A	ENSP00000384739.2:p.Pro136Thr
ENST00000526780.5:c.406C>A	ENSP00000435668.1:p.Pro136Thr
ENST00000527316.5:c.310C>A	ENSP00000435047.1:p.Pro104Thr
NM_001163817.1:c.406C>A	NP_001157289.1:p.Pro136Thr
NM_001360.2:c.406C>A , LRG_340t1:c.406C>A	NP_001351.2:p.Pro136Thr
XM_011544777.1:c.406C>A	XP_011543079.1:p.Pro136Thr
XM_011544777.2:c.406C>A	XP_011543079.1:p.Pro136Thr
NM_001163817.2:c.406C>A	NP_001157289.1:p.Pro136Thr
NM_001360.3:c.406C>A MANE Select	NP_001351.2:p.Pro136Thr