Canonical Allele Identifier: CA381701934

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71435679-G-A
• MyVariant Identifiers: chr11:g.71146725G>A (hg19) ; chr11:g.71435679G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435679G>A , CM000673.2:g.71435679G>A	GRCh38
NC_000011.9:g.71146725G>A , CM000673.1:g.71146725G>A	GRCh37
NC_000011.8:g.70824373G>A	NCBI36
NG_012655.2:g.17753C>T , LRG_340:g.17753C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1124C>T	ENSP00000435707.3:p.Pro375Leu
ENST00000526780.6:c.1124C>T	ENSP00000435668.2:p.Pro375Leu
ENST00000527316.6:c.950C>T	ENSP00000435047.2:p.Pro317Leu
ENST00000682708.1:c.1175C>T	ENSP00000506866.1:p.Pro392Leu
ENST00000683287.1:c.1160C>T	ENSP00000507607.1:p.Pro387Leu
ENST00000683714.1:c.1132C>T	ENSP00000508207.1:p.Pro378Ser
ENST00000684396.1:n.1164C>T
ENST00000685320.1:c.539C>T	ENSP00000509319.1:p.Pro180Leu
ENST00000690257.1:c.1028C>T	ENSP00000510750.1:p.Pro343Leu
ENST00000355527.8:c.1124C>T MANE Select	ENSP00000347717.4:p.Pro375Leu
ENST00000355527.7:c.1124C>T	ENSP00000347717.3:p.Pro375Leu
ENST00000407721.6:c.1124C>T	ENSP00000384739.2:p.Pro375Leu
ENST00000525137.1:c.625C>T	ENSP00000435956.1:p.Pro209Ser
ENST00000533800.5:c.374C>T	ENSP00000435011.1:p.Pro125Leu
ENST00000534795.5:c.319+2133C>T
NM_001163817.1:c.1124C>T	NP_001157289.1:p.Pro375Leu
NM_001360.2:c.1124C>T , LRG_340t1:c.1124C>T	NP_001351.2:p.Pro375Leu
XM_011544777.1:c.1258C>T	XP_011543079.1:p.Pro420Ser
XM_011544777.2:c.1258C>T	XP_011543079.1:p.Pro420Ser
NM_001163817.2:c.1124C>T	NP_001157289.1:p.Pro375Leu
NM_001360.3:c.1124C>T MANE Select	NP_001351.2:p.Pro375Leu