Canonical Allele Identifier: CA2758898377

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941850_150941857del , CM000665.2:g.150941850_150941857del	GRCh38
NC_000003.11:g.150659637_150659644del , CM000665.1:g.150659637_150659644del	GRCh37
NC_000003.10:g.152142327_152142334del	NCBI36
NG_009168.1:g.36144_36151del , LRG_700:g.36144_36151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.254-95_254-88del MANE Select	ENSP00000322280.1:n.254-95_254-88del
ENST00000468836.2:c.402-95_402-88del	ENSP00000419892.2:n.402-95_402-88del
ENST00000644099.1:c.246-95_246-88del	ENSP00000494762.1:n.246-95_246-88del
ENST00000295911.6:c.26-95_26-88del	ENSP00000295911.2:n.26-95_26-88del
ENST00000327047.5:c.254-95_254-88del	ENSP00000322280.1:n.254-95_254-88del
ENST00000328863.8:c.254-95_254-88del	ENSP00000329158.4:n.254-95_254-88del
ENST00000468836.1:c.26-95_26-88del	ENSP00000419892.1:n.26-95_26-88del
ENST00000472224.1:n.260-95_260-88del
ENST00000485607.1:c.-83-95_-83-88del	ENSP00000419244.1:n.-83-95_-83-88del
NM_001195794.1:c.254-95_254-88del , LRG_700t1:c.254-95_254-88del	NP_001182723.1:n.254-95_254-88del
NM_001256819.1:c.426-95_426-88del	NP_001243748.1:n.426-95_426-88del
NM_052995.2:c.26-95_26-88del , LRG_700t2:c.26-95_26-88del	NP_443721.1:n.26-95_26-88del
NM_174878.2:c.254-95_254-88del	NP_777367.1:n.254-95_254-88del
NR_046380.2:n.696-95_696-88del
XR_924167.1:n.566-95_566-88del
NM_001256819.2:c.426-95_426-88del	NP_001243748.1:n.426-95_426-88del
NM_174878.3:c.254-95_254-88del MANE Select	NP_777367.1:n.254-95_254-88del
NR_046380.3:n.424-95_424-88del