Canonical Allele Identifier: CA2666172

Gene: CLRN1

Linked Data

• dbSNP Id: rs777391431
• ExAC: 3:150690199 G / A
• gnomAD v2: 3-150690199-G-A
• gnomAD v3: 3-150972412-G-A
• gnomAD v4: 3-150972412-G-A
• MyVariant Identifiers: chr3:g.150690199G>A (hg19) ; chr3:g.150972412G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972412G>A , CM000665.2:g.150972412G>A	GRCh38
NC_000003.11:g.150690199G>A , CM000665.1:g.150690199G>A	GRCh37
NC_000003.10:g.152172889G>A	NCBI36
NG_009168.1:g.5588C>T , LRG_700:g.5588C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.253+44C>T MANE Select	ENSP00000322280.1:n.253+44C>T
ENST00000468836.2:c.229+44C>T	ENSP00000419892.2:n.229+44C>T
ENST00000644099.1:c.94+44C>T	ENSP00000494762.1:n.94+44C>T
ENST00000645441.1:c.95+44C>T
ENST00000327047.5:c.253+44C>T	ENSP00000322280.1:n.253+44C>T
ENST00000328863.8:c.253+44C>T	ENSP00000329158.4:n.253+44C>T
ENST00000468836.1:c.-148+44C>T	ENSP00000419892.1:n.-148+44C>T
ENST00000472224.1:n.259+44C>T
NM_001195794.1:c.253+44C>T , LRG_700t1:c.253+44C>T	NP_001182723.1:n.253+44C>T
NM_001256819.1:c.253+44C>T	NP_001243748.1:n.253+44C>T
NM_174878.2:c.253+44C>T	NP_777367.1:n.253+44C>T
NR_046380.2:n.544+44C>T
XR_924167.1:n.565+44C>T
NM_001256819.2:c.253+44C>T	NP_001243748.1:n.253+44C>T
NM_174878.3:c.253+44C>T MANE Select	NP_777367.1:n.253+44C>T
NR_046380.3:n.272+44C>T