Canonical Allele Identifier: CA1410883142
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150927874C= , CM000665.2:g.150927874C= GRCh38
NC_000003.11:g.150645661C= , CM000665.1:g.150645661C= GRCh37
NC_000003.10:g.152128351C= NCBI36
NG_009168.1:g.50126G= , LRG_700:g.50126G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.*62G= MANE Select ENSP00000322280.1:n.*62G=
ENST00000295911.6:c.342+191G= ENSP00000295911.2:n.342+191G=
ENST00000327047.5:c.*62G= ENSP00000322280.1:n.*62G=
ENST00000562308.5:c.104+13708G=
ENST00000565169.1:c.162+13708G=
ENST00000569170.5:c.162+13708G=
NM_001195794.1:c.*62G= , LRG_700t1:c.*62G= NP_001182723.1:n.*62G=
NM_001256819.1:c.*375G= NP_001243748.1:n.*375G=
NM_052995.2:c.342+191G= , LRG_700t2:c.342+191G= NP_443721.1:n.342+191G=
NM_174878.2:c.*62G= NP_777367.1:n.*62G=
NR_046380.2:n.1242G=
XR_924167.1:n.1073G=
NM_001256819.2:c.*375G= NP_001243748.1:n.*375G=
NM_174878.3:c.*62G= MANE Select NP_777367.1:n.*62G=
NR_046380.3:n.970G=