Canonical Allele Identifier: CA2772788941
Gene: CEP85L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118672532T>C , CM000668.2:g.118672532T>C GRCh38
NC_000006.11:g.118993695T>C , CM000668.1:g.118993695T>C GRCh37
NC_000006.10:g.119100388T>C NCBI36
NG_021248.1:g.42544A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368488.9:c.-27-19724A>G ENSP00000357474.5:n.-27-19724A>G
ENST00000392500.7:c.-138-8011A>G ENSP00000376288.3:n.-138-8011A>G
ENST00000434604.5:c.-27-19724A>G ENSP00000392131.1:n.-27-19724A>G
NM_001178035.1:c.-27-19724A>G NP_001171506.1:n.-27-19724A>G
XM_011535811.1:c.-234+37504A>G XP_011534113.1:n.-234+37504A>G
XR_942917.1:n.544+7382T>C
XR_942918.1:n.545-6712T>C
XM_011535810.2:c.-138-8011A>G XP_011534112.1:n.-138-8011A>G
XM_017010846.1:c.-138-8011A>G XP_016866335.1:n.-138-8011A>G
XM_024446429.1:c.-1650-8011A>G XP_024302197.1:n.-1650-8011A>G
XM_024446430.1:c.-1650-8011A>G XP_024302198.1:n.-1650-8011A>G
NM_001178035.2:c.-27-19724A>G NP_001171506.1:n.-27-19724A>G