Canonical Allele Identifier: CA436403122
Gene: CLRN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.150690385A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972598A>T , CM000665.2:g.150972598A>T GRCh38
NC_000003.11:g.150690385A>T , CM000665.1:g.150690385A>T GRCh37
NC_000003.10:g.152173075A>T NCBI36
NG_009168.1:g.5402T>A , LRG_700:g.5402T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.111T>A MANE Select ENSP00000322280.1:p.Thr37=
ENST00000468836.2:c.87T>A ENSP00000419892.2:p.Thr29=
ENST00000327047.5:c.111T>A ENSP00000322280.1:p.Thr37=
ENST00000328863.8:c.111T>A ENSP00000329158.4:p.Thr37=
ENST00000468836.1:c.-290T>A ENSP00000419892.1:n.-290T>A
ENST00000472224.1:n.117T>A
NM_001195794.1:c.111T>A , LRG_700t1:c.111T>A NP_001182723.1:p.Thr37=
NM_001256819.1:c.111T>A NP_001243748.1:p.Thr37=
NM_174878.2:c.111T>A NP_777367.1:p.Thr37=
NR_046380.2:n.402T>A
XR_924167.1:n.423T>A
NM_001256819.2:c.111T>A NP_001243748.1:p.Thr37=
NM_174878.3:c.111T>A MANE Select NP_777367.1:p.Thr37=
NR_046380.3:n.130T>A