Canonical Allele Identifier: CA547369177

Gene: CLRN1 CLRN1-AS1

Linked Data

• dbSNP Id: rs1347735033
• gnomAD v2: 3-150690505-C-T
• gnomAD v3: 3-150972718-C-T
• gnomAD v4: 3-150972718-C-T
• MyVariant Identifiers: chr3:g.150690505C>T (hg19) ; chr3:g.150972718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972718C>T , CM000665.2:g.150972718C>T	GRCh38
NC_000003.11:g.150690505C>T , CM000665.1:g.150690505C>T	GRCh37
NC_000003.10:g.152173195C>T	NCBI36
NG_009168.1:g.5282G>A , LRG_700:g.5282G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.-10G>A (CLRN1) MANE Select	ENSP00000322280.1:n.-10G>A
ENST00000327047.5:c.-10G>A (CLRN1)	ENSP00000322280.1:n.-10G>A
NM_001195794.1:c.-10G>A , LRG_700t1:c.-10G>A (CLRN1)	NP_001182723.1:n.-10G>A
NM_001256819.1:c.-10G>A (CLRN1)	NP_001243748.1:n.-10G>A
NM_174878.2:c.-10G>A (CLRN1)	NP_777367.1:n.-10G>A
NR_024066.1:n.41C>T (CLRN1-AS1)
NR_046380.2:n.282G>A (CLRN1)
XR_924167.1:n.303G>A (CLRN1)
NR_024066.2:n.41C>T (CLRN1-AS1)
NM_001256819.2:c.-10G>A (CLRN1)	NP_001243748.1:n.-10G>A
NM_174878.3:c.-10G>A (CLRN1) MANE Select	NP_777367.1:n.-10G>A
NR_046380.3:n.10G>A (CLRN1)