Canonical Allele Identifier: CA1410882613
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150926684C= , CM000665.2:g.150926684C= GRCh38
NC_000003.11:g.150644471C= , CM000665.1:g.150644471C= GRCh37
NC_000003.10:g.152127161C= NCBI36
NG_009168.1:g.51316G= , LRG_700:g.51316G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.*1252G= MANE Select ENSP00000322280.1:n.*1252G=
ENST00000295911.6:c.*168G= ENSP00000295911.2:n.*168G=
ENST00000327047.5:c.*1252G= ENSP00000322280.1:n.*1252G=
ENST00000562308.5:c.104+14898G=
ENST00000565169.1:c.162+14898G=
ENST00000569170.5:c.162+14898G=
NM_001195794.1:c.*1252G= , LRG_700t1:c.*1252G= NP_001182723.1:n.*1252G=
NM_001256819.1:c.*1565G= NP_001243748.1:n.*1565G=
NM_052995.2:c.*168G= , LRG_700t2:c.*168G= NP_443721.1:n.*168G=
NM_174878.2:c.*1252G= NP_777367.1:n.*1252G=
NR_046380.2:n.2432G=
XR_924167.1:n.2263G=
NM_001256819.2:c.*1565G= NP_001243748.1:n.*1565G=
NM_174878.3:c.*1252G= MANE Select NP_777367.1:n.*1252G=
NR_046380.3:n.2160G=