Canonical Allele Identifier: CA1410888632
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941924T= , CM000665.2:g.150941924T= GRCh38
NC_000003.11:g.150659711T= , CM000665.1:g.150659711T= GRCh37
NC_000003.10:g.152142401T= NCBI36
NG_009168.1:g.36076A= , LRG_700:g.36076A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-163A= MANE Select ENSP00000322280.1:n.254-163A=
ENST00000468836.2:c.402-163A= ENSP00000419892.2:n.402-163A=
ENST00000644099.1:c.246-163A= ENSP00000494762.1:n.246-163A=
ENST00000295911.6:c.26-163A= ENSP00000295911.2:n.26-163A=
ENST00000327047.5:c.254-163A= ENSP00000322280.1:n.254-163A=
ENST00000328863.8:c.254-163A= ENSP00000329158.4:n.254-163A=
ENST00000468836.1:c.26-163A= ENSP00000419892.1:n.26-163A=
ENST00000472224.1:n.260-163A=
ENST00000485607.1:c.-83-163A= ENSP00000419244.1:n.-83-163A=
NM_001195794.1:c.254-163A= , LRG_700t1:c.254-163A= NP_001182723.1:n.254-163A=
NM_001256819.1:c.426-163A= NP_001243748.1:n.426-163A=
NM_052995.2:c.26-163A= , LRG_700t2:c.26-163A= NP_443721.1:n.26-163A=
NM_174878.2:c.254-163A= NP_777367.1:n.254-163A=
NR_046380.2:n.696-163A=
XR_924167.1:n.566-163A=
NM_001256819.2:c.426-163A= NP_001243748.1:n.426-163A=
NM_174878.3:c.254-163A= MANE Select NP_777367.1:n.254-163A=
NR_046380.3:n.424-163A=