Canonical Allele Identifier: CA2668197388

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150927860-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927860A>T , CM000665.2:g.150927860A>T	GRCh38
NC_000003.11:g.150645647A>T , CM000665.1:g.150645647A>T	GRCh37
NC_000003.10:g.152128337A>T	NCBI36
NG_009168.1:g.50140T>A , LRG_700:g.50140T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*76T>A MANE Select	ENSP00000322280.1:n.*76T>A
ENST00000295911.6:c.342+205T>A	ENSP00000295911.2:n.342+205T>A
ENST00000327047.5:c.*76T>A	ENSP00000322280.1:n.*76T>A
ENST00000562308.5:c.104+13722T>A
ENST00000565169.1:c.162+13722T>A
ENST00000569170.5:c.162+13722T>A
NM_001195794.1:c.*76T>A , LRG_700t1:c.*76T>A	NP_001182723.1:n.*76T>A
NM_001256819.1:c.*389T>A	NP_001243748.1:n.*389T>A
NM_052995.2:c.342+205T>A , LRG_700t2:c.342+205T>A	NP_443721.1:n.342+205T>A
NM_174878.2:c.*76T>A	NP_777367.1:n.*76T>A
NR_046380.2:n.1256T>A
XR_924167.1:n.1087T>A
NM_001256819.2:c.*389T>A	NP_001243748.1:n.*389T>A
NM_174878.3:c.*76T>A MANE Select	NP_777367.1:n.*76T>A
NR_046380.3:n.984T>A