Canonical Allele Identifier: CA2668197378

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150927846-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927846T>G , CM000665.2:g.150927846T>G	GRCh38
NC_000003.11:g.150645633T>G , CM000665.1:g.150645633T>G	GRCh37
NC_000003.10:g.152128323T>G	NCBI36
NG_009168.1:g.50154A>C , LRG_700:g.50154A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*90A>C MANE Select	ENSP00000322280.1:n.*90A>C
ENST00000295911.6:c.342+219A>C	ENSP00000295911.2:n.342+219A>C
ENST00000327047.5:c.*90A>C	ENSP00000322280.1:n.*90A>C
ENST00000562308.5:c.104+13736A>C
ENST00000565169.1:c.162+13736A>C
ENST00000569170.5:c.162+13736A>C
NM_001195794.1:c.*90A>C , LRG_700t1:c.*90A>C	NP_001182723.1:n.*90A>C
NM_001256819.1:c.*403A>C	NP_001243748.1:n.*403A>C
NM_052995.2:c.342+219A>C , LRG_700t2:c.342+219A>C	NP_443721.1:n.342+219A>C
NM_174878.2:c.*90A>C	NP_777367.1:n.*90A>C
NR_046380.2:n.1270A>C
XR_924167.1:n.1101A>C
NM_001256819.2:c.*403A>C	NP_001243748.1:n.*403A>C
NM_174878.3:c.*90A>C MANE Select	NP_777367.1:n.*90A>C
NR_046380.3:n.998A>C