Canonical Allele Identifier: CA354956013

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659509T>A (hg19) ; chr3:g.150941722T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941722T>A , CM000665.2:g.150941722T>A	GRCh38
NC_000003.11:g.150659509T>A , CM000665.1:g.150659509T>A	GRCh37
NC_000003.10:g.152142199T>A	NCBI36
NG_009168.1:g.36278A>T , LRG_700:g.36278A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.293A>T MANE Select	ENSP00000322280.1:p.His98Leu
ENST00000468836.2:c.441A>T	ENSP00000419892.2:p.Pro147=
ENST00000644099.1:c.285A>T	ENSP00000494762.1:n.285A>T
ENST00000295911.6:c.65A>T	ENSP00000295911.2:p.His22Leu
ENST00000327047.5:c.293A>T	ENSP00000322280.1:p.His98Leu
ENST00000328863.8:c.293A>T	ENSP00000329158.4:p.His98Leu
ENST00000468836.1:c.65A>T	ENSP00000419892.1:p.His22Leu
ENST00000472224.1:n.299A>T
ENST00000485607.1:c.-44A>T	ENSP00000419244.1:n.-44A>T
ENST00000565169.1:c.22A>T
ENST00000569170.5:c.22A>T
NM_001195794.1:c.293A>T , LRG_700t1:c.293A>T	NP_001182723.1:p.His98Leu
NM_001256819.1:c.465A>T	NP_001243748.1:p.Pro155=
NM_052995.2:c.65A>T , LRG_700t2:c.65A>T	NP_443721.1:p.His22Leu
NM_174878.2:c.293A>T	NP_777367.1:p.His98Leu
NR_046380.2:n.735A>T
XR_924167.1:n.605A>T
NM_001256819.2:c.465A>T	NP_001243748.1:p.Pro155=
NM_174878.3:c.293A>T MANE Select	NP_777367.1:p.His98Leu
NR_046380.3:n.463A>T