Canonical Allele Identifier: CA1410910221

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972528T= , CM000665.2:g.150972528T=	GRCh38
NC_000003.11:g.150690315T= , CM000665.1:g.150690315T=	GRCh37
NC_000003.10:g.152173005T=	NCBI36
NG_009168.1:g.5472A= , LRG_700:g.5472A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.181A= MANE Select	ENSP00000322280.1:p.Met61=
ENST00000468836.2:c.157A=	ENSP00000419892.2:p.Met53=
ENST00000644099.1:c.22A=	ENSP00000494762.1:p.Met8=
ENST00000645441.1:c.23A=
ENST00000327047.5:c.181A=	ENSP00000322280.1:p.Met61=
ENST00000328863.8:c.181A=	ENSP00000329158.4:p.Met61=
ENST00000468836.1:c.-220A=	ENSP00000419892.1:n.-220A=
ENST00000472224.1:n.187A=
NM_001195794.1:c.181A= , LRG_700t1:c.181A=	NP_001182723.1:p.Met61=
NM_001256819.1:c.181A=	NP_001243748.1:p.Met61=
NM_174878.2:c.181A=	NP_777367.1:p.Met61=
NR_046380.2:n.472A=
XR_924167.1:n.493A=
NM_001256819.2:c.181A=	NP_001243748.1:p.Met61=
NM_174878.3:c.181A= MANE Select	NP_777367.1:p.Met61=
NR_046380.3:n.200A=