Canonical Allele Identifier: CA354952848

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150645766T>G (hg19) ; chr3:g.150927979T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927979T>G , CM000665.2:g.150927979T>G	GRCh38
NC_000003.11:g.150645766T>G , CM000665.1:g.150645766T>G	GRCh37
NC_000003.10:g.152128456T>G	NCBI36
NG_009168.1:g.50021A>C , LRG_700:g.50021A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.656A>C MANE Select	ENSP00000322280.1:p.Lys219Thr
ENST00000295911.6:c.342+86A>C	ENSP00000295911.2:n.342+86A>C
ENST00000327047.5:c.656A>C	ENSP00000322280.1:p.Lys219Thr
ENST00000328863.8:c.695A>C	ENSP00000329158.4:p.Lys232Thr
ENST00000562308.5:c.104+13603A>C
ENST00000565169.1:c.162+13603A>C
ENST00000569170.5:c.162+13603A>C
NM_001195794.1:c.695A>C , LRG_700t1:c.695A>C	NP_001182723.1:p.Lys232Thr
NM_001256819.1:c.*270A>C	NP_001243748.1:n.*270A>C
NM_052995.2:c.342+86A>C , LRG_700t2:c.342+86A>C	NP_443721.1:n.342+86A>C
NM_174878.2:c.656A>C	NP_777367.1:p.Lys219Thr
NR_046380.2:n.1137A>C
XR_924167.1:n.968A>C
NM_001256819.2:c.*270A>C	NP_001243748.1:n.*270A>C
NM_174878.3:c.656A>C MANE Select	NP_777367.1:p.Lys219Thr
NR_046380.3:n.865A>C