Canonical Allele Identifier: CA355011842

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690296T>G (hg19) ; chr3:g.150972509T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972509T>G , CM000665.2:g.150972509T>G	GRCh38
NC_000003.11:g.150690296T>G , CM000665.1:g.150690296T>G	GRCh37
NC_000003.10:g.152172986T>G	NCBI36
NG_009168.1:g.5491A>C , LRG_700:g.5491A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.200A>C MANE Select	ENSP00000322280.1:p.His67Pro
ENST00000468836.2:c.176A>C	ENSP00000419892.2:p.His59Pro
ENST00000644099.1:c.41A>C	ENSP00000494762.1:p.His14Pro
ENST00000645441.1:c.42A>C
ENST00000327047.5:c.200A>C	ENSP00000322280.1:p.His67Pro
ENST00000328863.8:c.200A>C	ENSP00000329158.4:p.His67Pro
ENST00000468836.1:c.-201A>C	ENSP00000419892.1:n.-201A>C
ENST00000472224.1:n.206A>C
NM_001195794.1:c.200A>C , LRG_700t1:c.200A>C	NP_001182723.1:p.His67Pro
NM_001256819.1:c.200A>C	NP_001243748.1:p.His67Pro
NM_174878.2:c.200A>C	NP_777367.1:p.His67Pro
NR_046380.2:n.491A>C
XR_924167.1:n.512A>C
NM_001256819.2:c.200A>C	NP_001243748.1:p.His67Pro
NM_174878.3:c.200A>C MANE Select	NP_777367.1:p.His67Pro
NR_046380.3:n.219A>C