Canonical Allele Identifier: CA1410888034
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150940843T= , CM000665.2:g.150940843T= GRCh38
NC_000003.11:g.150658630T= , CM000665.1:g.150658630T= GRCh37
NC_000003.10:g.152141320T= NCBI36
NG_009168.1:g.37157A= , LRG_700:g.37157A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.433+739A= MANE Select ENSP00000322280.1:n.433+739A=
ENST00000468836.2:c.581+739A= ENSP00000419892.2:n.581+739A=
ENST00000644099.1:c.426-324A= ENSP00000494762.1:n.426-324A=
ENST00000295911.6:c.205+739A= ENSP00000295911.2:n.205+739A=
ENST00000327047.5:c.433+739A= ENSP00000322280.1:n.433+739A=
ENST00000328863.8:c.434-324A= ENSP00000329158.4:n.434-324A=
ENST00000468836.1:c.205+739A= ENSP00000419892.1:n.205+739A=
ENST00000485607.1:c.97+739A= ENSP00000419244.1:n.97+739A=
ENST00000562308.5:c.104+739A=
ENST00000565169.1:c.162+739A=
ENST00000569170.5:c.162+739A=
NM_001195794.1:c.434-324A= , LRG_700t1:c.434-324A= NP_001182723.1:n.434-324A=
NM_001256819.1:c.*47+739A= NP_001243748.1:n.*47+739A=
NM_052995.2:c.205+739A= , LRG_700t2:c.205+739A= NP_443721.1:n.205+739A=
NM_174878.2:c.433+739A= NP_777367.1:n.433+739A=
NR_046380.2:n.876-324A=
XR_924167.1:n.745+739A=
NM_001256819.2:c.*47+739A= NP_001243748.1:n.*47+739A=
NM_174878.3:c.433+739A= MANE Select NP_777367.1:n.433+739A=
NR_046380.3:n.604-324A=