Canonical Allele Identifier: CA1410883241

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928107A= , CM000665.2:g.150928107A=	GRCh38
NC_000003.11:g.150645894A= , CM000665.1:g.150645894A=	GRCh37
NC_000003.10:g.152128584A=	NCBI36
NG_009168.1:g.49893T= , LRG_700:g.49893T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.528T= MANE Select	ENSP00000322280.1:p.Tyr176=
ENST00000468836.2:c.676T=	ENSP00000419892.2:n.676T=
ENST00000295911.6:c.300T=	ENSP00000295911.2:p.Tyr100=
ENST00000327047.5:c.528T=	ENSP00000322280.1:p.Tyr176=
ENST00000328863.8:c.567T=	ENSP00000329158.4:p.Tyr189=
ENST00000468836.1:c.300T=	ENSP00000419892.1:p.Tyr100=
ENST00000562308.5:c.104+13475T=
ENST00000565169.1:c.162+13475T=
ENST00000569170.5:c.162+13475T=
NM_001195794.1:c.567T= , LRG_700t1:c.567T=	NP_001182723.1:p.Tyr189=
NM_001256819.1:c.*142T=	NP_001243748.1:n.*142T=
NM_052995.2:c.300T= , LRG_700t2:c.300T=	NP_443721.1:p.Tyr100=
NM_174878.2:c.528T=	NP_777367.1:p.Tyr176=
NR_046380.2:n.1009T=
XR_924167.1:n.840T=
NM_001256819.2:c.*142T=	NP_001243748.1:n.*142T=
NM_174878.3:c.528T= MANE Select	NP_777367.1:p.Tyr176=
NR_046380.3:n.737T=