Canonical Allele Identifier: CA1658244450

Gene: CEP85L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118672402_118672404delinsCTA , CM000668.2:g.118672402_118672404delinsCTA	GRCh38
NC_000006.11:g.118993565_118993567delinsCTA , CM000668.1:g.118993565_118993567delinsCTA	GRCh37
NC_000006.10:g.119100258_119100260delinsCTA	NCBI36
NG_021248.1:g.42672_42674delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368488.9:c.-27-19596_-27-19594delinsTAG	ENSP00000357474.5:n.-27-19596_-27-19594delinsTAG
ENST00000392500.7:c.-138-7883_-138-7881delinsTAG	ENSP00000376288.3:n.-138-7883_-138-7881delinsTAG
ENST00000434604.5:c.-27-19596_-27-19594delinsTAG	ENSP00000392131.1:n.-27-19596_-27-19594delinsTAG
NM_001178035.1:c.-27-19596_-27-19594delinsTAG	NP_001171506.1:n.-27-19596_-27-19594delinsTAG
XM_011535811.1:c.-234+37632_-234+37634delinsTAG	XP_011534113.1:n.-234+37632_-234+37634delinsTAG
XR_942917.1:n.544+7252_544+7254delinsCTA
XR_942918.1:n.545-6842_545-6840delinsCTA
XM_011535810.2:c.-138-7883_-138-7881delinsTAG	XP_011534112.1:n.-138-7883_-138-7881delinsTAG
XM_017010846.1:c.-138-7883_-138-7881delinsTAG	XP_016866335.1:n.-138-7883_-138-7881delinsTAG
XM_024446429.1:c.-1650-7883_-1650-7881delinsTAG	XP_024302197.1:n.-1650-7883_-1650-7881delinsTAG
XM_024446430.1:c.-1650-7883_-1650-7881delinsTAG	XP_024302198.1:n.-1650-7883_-1650-7881delinsTAG
NM_001178035.2:c.-27-19596_-27-19594delinsTAG	NP_001171506.1:n.-27-19596_-27-19594delinsTAG