Canonical Allele Identifier: CA900656349

Gene: CLRN1

Linked Data

• dbSNP Id: rs1255344757
• MyVariant Identifiers: chr3:g.150643980_150643981insT (hg19) ; chr3:g.150926193_150926194insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926198dup , CM000665.2:g.150926198dup	GRCh38
NC_000003.11:g.150643985dup , CM000665.1:g.150643985dup	GRCh37
NC_000003.10:g.152126675dup	NCBI36
NG_009168.1:g.51806dup , LRG_700:g.51806dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295911.6:c.*658dup	ENSP00000295911.2:n.*658dup
ENST00000562308.5:c.104+15388dup
ENST00000565169.1:c.162+15388dup
ENST00000569170.5:c.162+15388dup
NM_052995.2:c.*658dup , LRG_700t2:c.*658dup	NP_443721.1:n.*658dup
XR_924167.1:n.2753dup