Canonical Allele Identifier: CA600039653

Gene: DHCR7

Linked Data

• dbSNP Id: rs542879175
• gnomAD v2: 11-71153430-C-G
• gnomAD v3: 11-71442384-C-G
• gnomAD v4: 11-71442384-C-G
• MyVariant Identifiers: chr11:g.71153430C>G (hg19) ; chr11:g.71442384C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71442384C>G , CM000673.2:g.71442384C>G	GRCh38
NC_000011.9:g.71153430C>G , CM000673.1:g.71153430C>G	GRCh37
NC_000011.8:g.70831078C>G	NCBI36
NG_012655.2:g.11048G>C , LRG_340:g.11048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.322-31G>C	ENSP00000435707.3:n.322-31G>C
ENST00000526780.6:c.322-31G>C	ENSP00000435668.2:n.322-31G>C
ENST00000527316.6:c.148-31G>C	ENSP00000435047.2:n.148-31G>C
ENST00000682708.1:c.322-31G>C	ENSP00000506866.1:n.322-31G>C
ENST00000682880.1:c.322-31G>C	ENSP00000507520.1:n.322-31G>C
ENST00000683287.1:c.358-31G>C	ENSP00000507607.1:n.358-31G>C
ENST00000683714.1:c.322-31G>C	ENSP00000508207.1:n.322-31G>C
ENST00000683874.1:n.599-31G>C
ENST00000685320.1:c.-264-31G>C	ENSP00000509319.1:n.-264-31G>C
ENST00000690257.1:c.226-31G>C	ENSP00000510750.1:n.226-31G>C
ENST00000355527.8:c.322-31G>C MANE Select	ENSP00000347717.4:n.322-31G>C
ENST00000355527.7:c.322-31G>C	ENSP00000347717.3:n.322-31G>C
ENST00000407721.6:c.322-31G>C	ENSP00000384739.2:n.322-31G>C
ENST00000526780.5:c.322-31G>C	ENSP00000435668.1:n.322-31G>C
ENST00000527316.5:c.226-31G>C	ENSP00000435047.1:n.226-31G>C
NM_001163817.1:c.322-31G>C	NP_001157289.1:n.322-31G>C
NM_001360.2:c.322-31G>C , LRG_340t1:c.322-31G>C	NP_001351.2:n.322-31G>C
XM_011544777.1:c.322-31G>C	XP_011543079.1:n.322-31G>C
XM_011544777.2:c.322-31G>C	XP_011543079.1:n.322-31G>C
NM_001163817.2:c.322-31G>C	NP_001157289.1:n.322-31G>C
NM_001360.3:c.322-31G>C MANE Select	NP_001351.2:n.322-31G>C