Canonical Allele Identifier: CA355011799

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150972489-A-G
• MyVariant Identifiers: chr3:g.150690276A>G (hg19) ; chr3:g.150972489A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972489A>G , CM000665.2:g.150972489A>G	GRCh38
NC_000003.11:g.150690276A>G , CM000665.1:g.150690276A>G	GRCh37
NC_000003.10:g.152172966A>G	NCBI36
NG_009168.1:g.5511T>C , LRG_700:g.5511T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.220T>C MANE Select	ENSP00000322280.1:p.Cys74Arg
ENST00000468836.2:c.196T>C	ENSP00000419892.2:p.Cys66Arg
ENST00000644099.1:c.61T>C	ENSP00000494762.1:p.Cys21Arg
ENST00000645441.1:c.62T>C
ENST00000327047.5:c.220T>C	ENSP00000322280.1:p.Cys74Arg
ENST00000328863.8:c.220T>C	ENSP00000329158.4:p.Cys74Arg
ENST00000468836.1:c.-181T>C	ENSP00000419892.1:n.-181T>C
ENST00000472224.1:n.226T>C
NM_001195794.1:c.220T>C , LRG_700t1:c.220T>C	NP_001182723.1:p.Cys74Arg
NM_001256819.1:c.220T>C	NP_001243748.1:p.Cys74Arg
NM_174878.2:c.220T>C	NP_777367.1:p.Cys74Arg
NR_046380.2:n.511T>C
XR_924167.1:n.532T>C
NM_001256819.2:c.220T>C	NP_001243748.1:p.Cys74Arg
NM_174878.3:c.220T>C MANE Select	NP_777367.1:p.Cys74Arg
NR_046380.3:n.239T>C