Canonical Allele Identifier: CA16277783

Gene: CEP85L

Linked Data

• ClinVar Variation Id: 403328
• ClinVar RCV Id: RCV001516345 ; RCV001637028 ; RCV001803752
• dbSNP Id: rs77186188
• gnomAD v2: 6-118869423-A-C
• gnomAD v3: 6-118548260-A-C
• gnomAD v4: 6-118548260-A-C
• MyVariant Identifiers: chr6:g.118869423A>C (hg19) ; chr6:g.118548260A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118548260A>C , CM000668.2:g.118548260A>C	GRCh38
NC_000006.11:g.118869423A>C , CM000668.1:g.118869423A>C	GRCh37
NC_000006.10:g.118976116A>C	NCBI36
NG_009082.1:g.4982A>C , LRG_390:g.4982A>C
NG_021248.1:g.166816T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368491.8:c.1020+17269T>G MANE Select	ENSP00000357477.3:n.1020+17269T>G
ENST00000360290.7:c.714+17269T>G	ENSP00000353434.3:n.714+17269T>G
ENST00000368488.9:c.1029+17269T>G	ENSP00000357474.5:n.1029+17269T>G
ENST00000368491.7:c.1020+17269T>G	ENSP00000357477.3:n.1020+17269T>G
ENST00000392500.7:c.1029+17269T>G	ENSP00000376288.3:n.1029+17269T>G
ENST00000419517.2:c.1020+17269T>G	ENSP00000393317.2:n.1020+17269T>G
ENST00000434604.5:c.1029+17269T>G	ENSP00000392131.1:n.1029+17269T>G
NM_001042475.2:c.1020+17269T>G	NP_001035940.1:n.1020+17269T>G
NM_001178035.1:c.1029+17269T>G	NP_001171506.1:n.1029+17269T>G
NM_206921.2:c.1020+17269T>G	NP_996804.2:n.1020+17269T>G
XM_005266970.1:c.714+17269T>G	XP_005267027.1:n.714+17269T>G
XM_005266971.1:c.714+17269T>G	XP_005267028.1:n.714+17269T>G
XM_006715475.2:c.714+17269T>G	XP_006715538.1:n.714+17269T>G
XM_011535808.1:c.1029+17269T>G	XP_011534110.1:n.1029+17269T>G
XM_011535809.1:c.1020+17269T>G	XP_011534111.1:n.1020+17269T>G
XM_011535810.1:c.1029+17269T>G	XP_011534112.1:n.1029+17269T>G
XM_011535811.1:c.714+17269T>G	XP_011534113.1:n.714+17269T>G
XM_011535812.1:c.-67+15676T>G	XP_011534114.1:n.-67+15676T>G
XM_006715475.4:c.714+17269T>G	XP_006715538.1:n.714+17269T>G
XM_011535809.2:c.1020+17269T>G	XP_011534111.1:n.1020+17269T>G
XM_011535810.2:c.1029+17269T>G	XP_011534112.1:n.1029+17269T>G
XM_017010846.1:c.1029+17269T>G	XP_016866335.1:n.1029+17269T>G
XM_024446429.1:c.1020+17269T>G	XP_024302197.1:n.1020+17269T>G
XM_024446430.1:c.1020+17269T>G	XP_024302198.1:n.1020+17269T>G
NM_001042475.3:c.1020+17269T>G MANE Select	NP_001035940.1:n.1020+17269T>G
NM_206921.3:c.1020+17269T>G	NP_996804.2:n.1020+17269T>G
NM_001178035.2:c.1029+17269T>G	NP_001171506.1:n.1029+17269T>G