Canonical Allele Identifier: CA2668197393

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150927876-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927876A>T , CM000665.2:g.150927876A>T	GRCh38
NC_000003.11:g.150645663A>T , CM000665.1:g.150645663A>T	GRCh37
NC_000003.10:g.152128353A>T	NCBI36
NG_009168.1:g.50124T>A , LRG_700:g.50124T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.*60T>A MANE Select	ENSP00000322280.1:n.*60T>A
ENST00000295911.6:c.342+189T>A	ENSP00000295911.2:n.342+189T>A
ENST00000327047.5:c.*60T>A	ENSP00000322280.1:n.*60T>A
ENST00000562308.5:c.104+13706T>A
ENST00000565169.1:c.162+13706T>A
ENST00000569170.5:c.162+13706T>A
NM_001195794.1:c.*60T>A , LRG_700t1:c.*60T>A	NP_001182723.1:n.*60T>A
NM_001256819.1:c.*373T>A	NP_001243748.1:n.*373T>A
NM_052995.2:c.342+189T>A , LRG_700t2:c.342+189T>A	NP_443721.1:n.342+189T>A
NM_174878.2:c.*60T>A	NP_777367.1:n.*60T>A
NR_046380.2:n.1240T>A
XR_924167.1:n.1071T>A
NM_001256819.2:c.*373T>A	NP_001243748.1:n.*373T>A
NM_174878.3:c.*60T>A MANE Select	NP_777367.1:n.*60T>A
NR_046380.3:n.968T>A