Canonical Allele Identifier: CA817886286

Gene: CEP85L

Linked Data

• dbSNP Id: rs1479130627
• MyVariant Identifiers: chr6:g.118993657T>C (hg19) ; chr6:g.118672494T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118672494T>C , CM000668.2:g.118672494T>C	GRCh38
NC_000006.11:g.118993657T>C , CM000668.1:g.118993657T>C	GRCh37
NC_000006.10:g.119100350T>C	NCBI36
NG_021248.1:g.42582A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368488.9:c.-27-19686A>G	ENSP00000357474.5:n.-27-19686A>G
ENST00000392500.7:c.-138-7973A>G	ENSP00000376288.3:n.-138-7973A>G
ENST00000434604.5:c.-27-19686A>G	ENSP00000392131.1:n.-27-19686A>G
NM_001178035.1:c.-27-19686A>G	NP_001171506.1:n.-27-19686A>G
XM_011535811.1:c.-234+37542A>G	XP_011534113.1:n.-234+37542A>G
XR_942917.1:n.544+7344T>C
XR_942918.1:n.545-6750T>C
XM_011535810.2:c.-138-7973A>G	XP_011534112.1:n.-138-7973A>G
XM_017010846.1:c.-138-7973A>G	XP_016866335.1:n.-138-7973A>G
XM_024446429.1:c.-1650-7973A>G	XP_024302197.1:n.-1650-7973A>G
XM_024446430.1:c.-1650-7973A>G	XP_024302198.1:n.-1650-7973A>G
NM_001178035.2:c.-27-19686A>G	NP_001171506.1:n.-27-19686A>G