Canonical Allele Identifier: CA1410910163

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972414C= , CM000665.2:g.150972414C=	GRCh38
NC_000003.11:g.150690201C= , CM000665.1:g.150690201C=	GRCh37
NC_000003.10:g.152172891C=	NCBI36
NG_009168.1:g.5586G= , LRG_700:g.5586G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.253+42G= MANE Select	ENSP00000322280.1:n.253+42G=
ENST00000468836.2:c.229+42G=	ENSP00000419892.2:n.229+42G=
ENST00000644099.1:c.94+42G=	ENSP00000494762.1:n.94+42G=
ENST00000645441.1:c.95+42G=
ENST00000327047.5:c.253+42G=	ENSP00000322280.1:n.253+42G=
ENST00000328863.8:c.253+42G=	ENSP00000329158.4:n.253+42G=
ENST00000468836.1:c.-148+42G=	ENSP00000419892.1:n.-148+42G=
ENST00000472224.1:n.259+42G=
NM_001195794.1:c.253+42G= , LRG_700t1:c.253+42G=	NP_001182723.1:n.253+42G=
NM_001256819.1:c.253+42G=	NP_001243748.1:n.253+42G=
NM_174878.2:c.253+42G=	NP_777367.1:n.253+42G=
NR_046380.2:n.544+42G=
XR_924167.1:n.565+42G=
NM_001256819.2:c.253+42G=	NP_001243748.1:n.253+42G=
NM_174878.3:c.253+42G= MANE Select	NP_777367.1:n.253+42G=
NR_046380.3:n.272+42G=