Canonical Allele Identifier: CA354955578

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659447A>C (hg19) ; chr3:g.150941660A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941660A>C , CM000665.2:g.150941660A>C	GRCh38
NC_000003.11:g.150659447A>C , CM000665.1:g.150659447A>C	GRCh37
NC_000003.10:g.152142137A>C	NCBI36
NG_009168.1:g.36340T>G , LRG_700:g.36340T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.355T>G MANE Select	ENSP00000322280.1:p.Phe119Val
ENST00000468836.2:c.503T>G	ENSP00000419892.2:p.Leu168Arg
ENST00000644099.1:c.347T>G	ENSP00000494762.1:n.347T>G
ENST00000295911.6:c.127T>G	ENSP00000295911.2:p.Phe43Val
ENST00000327047.5:c.355T>G	ENSP00000322280.1:p.Phe119Val
ENST00000328863.8:c.355T>G	ENSP00000329158.4:p.Phe119Val
ENST00000468836.1:c.127T>G	ENSP00000419892.1:p.Phe43Val
ENST00000472224.1:n.361T>G
ENST00000485607.1:c.19T>G	ENSP00000419244.1:p.Phe7Val
ENST00000562308.5:c.26T>G
ENST00000565169.1:c.84T>G
ENST00000569170.5:c.84T>G
NM_001195794.1:c.355T>G , LRG_700t1:c.355T>G	NP_001182723.1:p.Phe119Val
NM_001256819.1:c.527T>G	NP_001243748.1:p.Leu176Arg
NM_052995.2:c.127T>G , LRG_700t2:c.127T>G	NP_443721.1:p.Phe43Val
NM_174878.2:c.355T>G	NP_777367.1:p.Phe119Val
NR_046380.2:n.797T>G
XR_924167.1:n.667T>G
NM_001256819.2:c.527T>G	NP_001243748.1:p.Leu176Arg
NM_174878.3:c.355T>G MANE Select	NP_777367.1:p.Phe119Val
NR_046380.3:n.525T>G