Canonical Allele Identifier: CA1410910278

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972629G= , CM000665.2:g.150972629G=	GRCh38
NC_000003.11:g.150690416G= , CM000665.1:g.150690416G=	GRCh37
NC_000003.10:g.152173106G=	NCBI36
NG_009168.1:g.5371C= , LRG_700:g.5371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.80C= MANE Select	ENSP00000322280.1:p.Ala27=
ENST00000468836.2:c.56C=	ENSP00000419892.2:p.Ala19=
ENST00000327047.5:c.80C=	ENSP00000322280.1:p.Ala27=
ENST00000328863.8:c.80C=	ENSP00000329158.4:p.Ala27=
ENST00000468836.1:c.-321C=	ENSP00000419892.1:n.-321C=
ENST00000472224.1:n.86C=
NM_001195794.1:c.80C= , LRG_700t1:c.80C=	NP_001182723.1:p.Ala27=
NM_001256819.1:c.80C=	NP_001243748.1:p.Ala27=
NM_174878.2:c.80C=	NP_777367.1:p.Ala27=
NR_046380.2:n.371C=
XR_924167.1:n.392C=
NM_001256819.2:c.80C=	NP_001243748.1:p.Ala27=
NM_174878.3:c.80C= MANE Select	NP_777367.1:p.Ala27=
NR_046380.3:n.99C=