Canonical Allele Identifier: CA355011883

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690314A>T (hg19) ; chr3:g.150972527A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972527A>T , CM000665.2:g.150972527A>T	GRCh38
NC_000003.11:g.150690314A>T , CM000665.1:g.150690314A>T	GRCh37
NC_000003.10:g.152173004A>T	NCBI36
NG_009168.1:g.5473T>A , LRG_700:g.5473T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.182T>A MANE Select	ENSP00000322280.1:p.Met61Lys
ENST00000468836.2:c.158T>A	ENSP00000419892.2:p.Met53Lys
ENST00000644099.1:c.23T>A	ENSP00000494762.1:p.Met8Lys
ENST00000645441.1:c.24T>A
ENST00000327047.5:c.182T>A	ENSP00000322280.1:p.Met61Lys
ENST00000328863.8:c.182T>A	ENSP00000329158.4:p.Met61Lys
ENST00000468836.1:c.-219T>A	ENSP00000419892.1:n.-219T>A
ENST00000472224.1:n.188T>A
NM_001195794.1:c.182T>A , LRG_700t1:c.182T>A	NP_001182723.1:p.Met61Lys
NM_001256819.1:c.182T>A	NP_001243748.1:p.Met61Lys
NM_174878.2:c.182T>A	NP_777367.1:p.Met61Lys
NR_046380.2:n.473T>A
XR_924167.1:n.494T>A
NM_001256819.2:c.182T>A	NP_001243748.1:p.Met61Lys
NM_174878.3:c.182T>A MANE Select	NP_777367.1:p.Met61Lys
NR_046380.3:n.201T>A