Canonical Allele Identifier: CA1410883231

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928082A= , CM000665.2:g.150928082A=	GRCh38
NC_000003.11:g.150645869A= , CM000665.1:g.150645869A=	GRCh37
NC_000003.10:g.152128559A=	NCBI36
NG_009168.1:g.49918T= , LRG_700:g.49918T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.553T= MANE Select	ENSP00000322280.1:p.Tyr185=
ENST00000468836.2:c.701T=	ENSP00000419892.2:n.701T=
ENST00000295911.6:c.325T=	ENSP00000295911.2:p.Tyr109=
ENST00000327047.5:c.553T=	ENSP00000322280.1:p.Tyr185=
ENST00000328863.8:c.592T=	ENSP00000329158.4:p.Tyr198=
ENST00000468836.1:c.325T=	ENSP00000419892.1:p.Tyr109=
ENST00000562308.5:c.104+13500T=
ENST00000565169.1:c.162+13500T=
ENST00000569170.5:c.162+13500T=
NM_001195794.1:c.592T= , LRG_700t1:c.592T=	NP_001182723.1:p.Tyr198=
NM_001256819.1:c.*167T=	NP_001243748.1:n.*167T=
NM_052995.2:c.325T= , LRG_700t2:c.325T=	NP_443721.1:p.Tyr109=
NM_174878.2:c.553T=	NP_777367.1:p.Tyr185=
NR_046380.2:n.1034T=
XR_924167.1:n.865T=
NM_001256819.2:c.*167T=	NP_001243748.1:n.*167T=
NM_174878.3:c.553T= MANE Select	NP_777367.1:p.Tyr185=
NR_046380.3:n.762T=