Canonical Allele Identifier: CA1410888611
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941890_150941894delinsCACTT , CM000665.2:g.150941890_150941894delinsCACTT GRCh38
NC_000003.11:g.150659677_150659681delinsCACTT , CM000665.1:g.150659677_150659681delinsCACTT GRCh37
NC_000003.10:g.152142367_152142371delinsCACTT NCBI36
NG_009168.1:g.36106_36110delinsAAGTG , LRG_700:g.36106_36110delinsAAGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-133_254-129delinsAAGTG MANE Select ENSP00000322280.1:n.254-133_254-129delinsAAGTG
ENST00000468836.2:c.402-133_402-129delinsAAGTG ENSP00000419892.2:n.402-133_402-129delinsAAGTG
ENST00000644099.1:c.246-133_246-129delinsAAGTG ENSP00000494762.1:n.246-133_246-129delinsAAGTG
ENST00000295911.6:c.26-133_26-129delinsAAGTG ENSP00000295911.2:n.26-133_26-129delinsAAGTG
ENST00000327047.5:c.254-133_254-129delinsAAGTG ENSP00000322280.1:n.254-133_254-129delinsAAGTG
ENST00000328863.8:c.254-133_254-129delinsAAGTG ENSP00000329158.4:n.254-133_254-129delinsAAGTG
ENST00000468836.1:c.26-133_26-129delinsAAGTG ENSP00000419892.1:n.26-133_26-129delinsAAGTG
ENST00000472224.1:n.260-133_260-129delinsAAGTG
ENST00000485607.1:c.-83-133_-83-129delinsAAGTG ENSP00000419244.1:n.-83-133_-83-129delinsAAGTG
NM_001195794.1:c.254-133_254-129delinsAAGTG , LRG_700t1:c.254-133_254-129delinsAAGTG NP_001182723.1:n.254-133_254-129delinsAAGTG
NM_001256819.1:c.426-133_426-129delinsAAGTG NP_001243748.1:n.426-133_426-129delinsAAGTG
NM_052995.2:c.26-133_26-129delinsAAGTG , LRG_700t2:c.26-133_26-129delinsAAGTG NP_443721.1:n.26-133_26-129delinsAAGTG
NM_174878.2:c.254-133_254-129delinsAAGTG NP_777367.1:n.254-133_254-129delinsAAGTG
NR_046380.2:n.696-133_696-129delinsAAGTG
XR_924167.1:n.566-133_566-129delinsAAGTG
NM_001256819.2:c.426-133_426-129delinsAAGTG NP_001243748.1:n.426-133_426-129delinsAAGTG
NM_174878.3:c.254-133_254-129delinsAAGTG MANE Select NP_777367.1:n.254-133_254-129delinsAAGTG
NR_046380.3:n.424-133_424-129delinsAAGTG