Canonical Allele Identifier: CA1410882652

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926786C= , CM000665.2:g.150926786C=	GRCh38
NC_000003.11:g.150644573C= , CM000665.1:g.150644573C=	GRCh37
NC_000003.10:g.152127263C=	NCBI36
NG_009168.1:g.51214G= , LRG_700:g.51214G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1150G= MANE Select	ENSP00000322280.1:n.*1150G=
ENST00000295911.6:c.*66G=	ENSP00000295911.2:n.*66G=
ENST00000327047.5:c.*1150G=	ENSP00000322280.1:n.*1150G=
ENST00000562308.5:c.104+14796G=
ENST00000565169.1:c.162+14796G=
ENST00000569170.5:c.162+14796G=
NM_001195794.1:c.*1150G= , LRG_700t1:c.*1150G=	NP_001182723.1:n.*1150G=
NM_001256819.1:c.*1463G=	NP_001243748.1:n.*1463G=
NM_052995.2:c.*66G= , LRG_700t2:c.*66G=	NP_443721.1:n.*66G=
NM_174878.2:c.*1150G=	NP_777367.1:n.*1150G=
NR_046380.2:n.2330G=
XR_924167.1:n.2161G=
NM_001256819.2:c.*1463G=	NP_001243748.1:n.*1463G=
NM_174878.3:c.*1150G= MANE Select	NP_777367.1:n.*1150G=
NR_046380.3:n.2058G=