Canonical Allele Identifier: CA1410910198

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972480C= , CM000665.2:g.150972480C=	GRCh38
NC_000003.11:g.150690267C= , CM000665.1:g.150690267C=	GRCh37
NC_000003.10:g.152172957C=	NCBI36
NG_009168.1:g.5520G= , LRG_700:g.5520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.229G= MANE Select	ENSP00000322280.1:p.Gly77=
ENST00000468836.2:c.205G=	ENSP00000419892.2:p.Gly69=
ENST00000644099.1:c.70G=	ENSP00000494762.1:p.Gly24=
ENST00000645441.1:c.71G=
ENST00000327047.5:c.229G=	ENSP00000322280.1:p.Gly77=
ENST00000328863.8:c.229G=	ENSP00000329158.4:p.Gly77=
ENST00000468836.1:c.-172G=	ENSP00000419892.1:n.-172G=
ENST00000472224.1:n.235G=
NM_001195794.1:c.229G= , LRG_700t1:c.229G=	NP_001182723.1:p.Gly77=
NM_001256819.1:c.229G=	NP_001243748.1:p.Gly77=
NM_174878.2:c.229G=	NP_777367.1:p.Gly77=
NR_046380.2:n.520G=
XR_924167.1:n.541G=
NM_001256819.2:c.229G=	NP_001243748.1:p.Gly77=
NM_174878.3:c.229G= MANE Select	NP_777367.1:p.Gly77=
NR_046380.3:n.248G=