Canonical Allele Identifier: CA436265242

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659399G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941612G>A , CM000665.2:g.150941612G>A	GRCh38
NC_000003.11:g.150659399G>A , CM000665.1:g.150659399G>A	GRCh37
NC_000003.10:g.152142089G>A	NCBI36
NG_009168.1:g.36388C>T , LRG_700:g.36388C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.403C>T MANE Select	ENSP00000322280.1:p.Leu135=
ENST00000468836.2:c.551C>T	ENSP00000419892.2:n.551C>T
ENST00000644099.1:c.395C>T	ENSP00000494762.1:n.395C>T
ENST00000295911.6:c.175C>T	ENSP00000295911.2:p.Leu59=
ENST00000327047.5:c.403C>T	ENSP00000322280.1:p.Leu135=
ENST00000328863.8:c.403C>T	ENSP00000329158.4:p.Leu135=
ENST00000468836.1:c.175C>T	ENSP00000419892.1:p.Leu59=
ENST00000472224.1:n.409C>T
ENST00000485607.1:c.67C>T	ENSP00000419244.1:p.Leu23=
ENST00000562308.5:c.74C>T
ENST00000565169.1:c.132C>T
ENST00000569170.5:c.132C>T
NM_001195794.1:c.403C>T , LRG_700t1:c.403C>T	NP_001182723.1:p.Leu135=
NM_001256819.1:c.*17C>T	NP_001243748.1:n.*17C>T
NM_052995.2:c.175C>T , LRG_700t2:c.175C>T	NP_443721.1:p.Leu59=
NM_174878.2:c.403C>T	NP_777367.1:p.Leu135=
NR_046380.2:n.845C>T
XR_924167.1:n.715C>T
NM_001256819.2:c.*17C>T	NP_001243748.1:n.*17C>T
NM_174878.3:c.403C>T MANE Select	NP_777367.1:p.Leu135=
NR_046380.3:n.573C>T