Canonical Allele Identifier: CA2758898359

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941818del , CM000665.2:g.150941818del	GRCh38
NC_000003.11:g.150659605del , CM000665.1:g.150659605del	GRCh37
NC_000003.10:g.152142295del	NCBI36
NG_009168.1:g.36182del , LRG_700:g.36182del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.254-57del MANE Select	ENSP00000322280.1:n.254-57del
ENST00000468836.2:c.402-57del	ENSP00000419892.2:n.402-57del
ENST00000644099.1:c.246-57del	ENSP00000494762.1:n.246-57del
ENST00000295911.6:c.26-57del	ENSP00000295911.2:n.26-57del
ENST00000327047.5:c.254-57del	ENSP00000322280.1:n.254-57del
ENST00000328863.8:c.254-57del	ENSP00000329158.4:n.254-57del
ENST00000468836.1:c.26-57del	ENSP00000419892.1:n.26-57del
ENST00000472224.1:n.260-57del
ENST00000485607.1:c.-83-57del	ENSP00000419244.1:n.-83-57del
NM_001195794.1:c.254-57del , LRG_700t1:c.254-57del	NP_001182723.1:n.254-57del
NM_001256819.1:c.426-57del	NP_001243748.1:n.426-57del
NM_052995.2:c.26-57del , LRG_700t2:c.26-57del	NP_443721.1:n.26-57del
NM_174878.2:c.254-57del	NP_777367.1:n.254-57del
NR_046380.2:n.696-57del
XR_924167.1:n.566-57del
NM_001256819.2:c.426-57del	NP_001243748.1:n.426-57del
NM_174878.3:c.254-57del MANE Select	NP_777367.1:n.254-57del
NR_046380.3:n.424-57del