Canonical Allele Identifier: CA355012008
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972588T>A , CM000665.2:g.150972588T>A GRCh38
NC_000003.11:g.150690375T>A , CM000665.1:g.150690375T>A GRCh37
NC_000003.10:g.152173065T>A NCBI36
NG_009168.1:g.5412A>T , LRG_700:g.5412A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.121A>T MANE Select ENSP00000322280.1:p.Lys41Ter
ENST00000468836.2:c.97A>T ENSP00000419892.2:p.Lys33Ter
ENST00000327047.5:c.121A>T ENSP00000322280.1:p.Lys41Ter
ENST00000328863.8:c.121A>T ENSP00000329158.4:p.Lys41Ter
ENST00000468836.1:c.-280A>T ENSP00000419892.1:n.-280A>T
ENST00000472224.1:n.127A>T
NM_001195794.1:c.121A>T , LRG_700t1:c.121A>T NP_001182723.1:p.Lys41Ter
NM_001256819.1:c.121A>T NP_001243748.1:p.Lys41Ter
NM_174878.2:c.121A>T NP_777367.1:p.Lys41Ter
NR_046380.2:n.412A>T
XR_924167.1:n.433A>T
NM_001256819.2:c.121A>T NP_001243748.1:p.Lys41Ter
NM_174878.3:c.121A>T MANE Select NP_777367.1:p.Lys41Ter
NR_046380.3:n.140A>T