Canonical Allele Identifier: CA1658244499

Gene: CEP85L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118672513T= , CM000668.2:g.118672513T=	GRCh38
NC_000006.11:g.118993676T= , CM000668.1:g.118993676T=	GRCh37
NC_000006.10:g.119100369T=	NCBI36
NG_021248.1:g.42563A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368488.9:c.-27-19705A=	ENSP00000357474.5:n.-27-19705A=
ENST00000392500.7:c.-138-7992A=	ENSP00000376288.3:n.-138-7992A=
ENST00000434604.5:c.-27-19705A=	ENSP00000392131.1:n.-27-19705A=
NM_001178035.1:c.-27-19705A=	NP_001171506.1:n.-27-19705A=
XM_011535811.1:c.-234+37523A=	XP_011534113.1:n.-234+37523A=
XR_942917.1:n.544+7363T=
XR_942918.1:n.545-6731T=
XM_011535810.2:c.-138-7992A=	XP_011534112.1:n.-138-7992A=
XM_017010846.1:c.-138-7992A=	XP_016866335.1:n.-138-7992A=
XM_024446429.1:c.-1650-7992A=	XP_024302197.1:n.-1650-7992A=
XM_024446430.1:c.-1650-7992A=	XP_024302198.1:n.-1650-7992A=
NM_001178035.2:c.-27-19705A=	NP_001171506.1:n.-27-19705A=