Canonical Allele Identifier: CA1410888470

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941591A= , CM000665.2:g.150941591A=	GRCh38
NC_000003.11:g.150659378A= , CM000665.1:g.150659378A=	GRCh37
NC_000003.10:g.152142068A=	NCBI36
NG_009168.1:g.36409T= , LRG_700:g.36409T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.424T= MANE Select	ENSP00000322280.1:p.Phe142=
ENST00000468836.2:c.572T=	ENSP00000419892.2:n.572T=
ENST00000644099.1:c.416T=	ENSP00000494762.1:n.416T=
ENST00000295911.6:c.196T=	ENSP00000295911.2:p.Phe66=
ENST00000327047.5:c.424T=	ENSP00000322280.1:p.Phe142=
ENST00000328863.8:c.424T=	ENSP00000329158.4:p.Phe142=
ENST00000468836.1:c.196T=	ENSP00000419892.1:p.Phe66=
ENST00000472224.1:n.430T=
ENST00000485607.1:c.88T=	ENSP00000419244.1:p.Phe30=
ENST00000562308.5:c.95T=
ENST00000565169.1:c.153T=
ENST00000569170.5:c.153T=
NM_001195794.1:c.424T= , LRG_700t1:c.424T=	NP_001182723.1:p.Phe142=
NM_001256819.1:c.*38T=	NP_001243748.1:n.*38T=
NM_052995.2:c.196T= , LRG_700t2:c.196T=	NP_443721.1:p.Phe66=
NM_174878.2:c.424T=	NP_777367.1:p.Phe142=
NR_046380.2:n.866T=
XR_924167.1:n.736T=
NM_001256819.2:c.*38T=	NP_001243748.1:n.*38T=
NM_174878.3:c.424T= MANE Select	NP_777367.1:p.Phe142=
NR_046380.3:n.594T=