Canonical Allele Identifier: CA436402980

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690304C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972517C>A , CM000665.2:g.150972517C>A	GRCh38
NC_000003.11:g.150690304C>A , CM000665.1:g.150690304C>A	GRCh37
NC_000003.10:g.152172994C>A	NCBI36
NG_009168.1:g.5483G>T , LRG_700:g.5483G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.192G>T MANE Select	ENSP00000322280.1:p.Gly64=
ENST00000468836.2:c.168G>T	ENSP00000419892.2:p.Gly56=
ENST00000644099.1:c.33G>T	ENSP00000494762.1:p.Gly11=
ENST00000645441.1:c.34G>T
ENST00000327047.5:c.192G>T	ENSP00000322280.1:p.Gly64=
ENST00000328863.8:c.192G>T	ENSP00000329158.4:p.Gly64=
ENST00000468836.1:c.-209G>T	ENSP00000419892.1:n.-209G>T
ENST00000472224.1:n.198G>T
NM_001195794.1:c.192G>T , LRG_700t1:c.192G>T	NP_001182723.1:p.Gly64=
NM_001256819.1:c.192G>T	NP_001243748.1:p.Gly64=
NM_174878.2:c.192G>T	NP_777367.1:p.Gly64=
NR_046380.2:n.483G>T
XR_924167.1:n.504G>T
NM_001256819.2:c.192G>T	NP_001243748.1:p.Gly64=
NM_174878.3:c.192G>T MANE Select	NP_777367.1:p.Gly64=
NR_046380.3:n.211G>T