Canonical Allele Identifier: CA436265494

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659526T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941739T>A , CM000665.2:g.150941739T>A	GRCh38
NC_000003.11:g.150659526T>A , CM000665.1:g.150659526T>A	GRCh37
NC_000003.10:g.152142216T>A	NCBI36
NG_009168.1:g.36261A>T , LRG_700:g.36261A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.276A>T MANE Select	ENSP00000322280.1:p.Ala92=
ENST00000468836.2:c.424A>T	ENSP00000419892.2:p.Asn142Tyr
ENST00000644099.1:c.268A>T	ENSP00000494762.1:n.268A>T
ENST00000295911.6:c.48A>T	ENSP00000295911.2:p.Ala16=
ENST00000327047.5:c.276A>T	ENSP00000322280.1:p.Ala92=
ENST00000328863.8:c.276A>T	ENSP00000329158.4:p.Ala92=
ENST00000468836.1:c.48A>T	ENSP00000419892.1:p.Ala16=
ENST00000472224.1:n.282A>T
ENST00000485607.1:c.-61A>T	ENSP00000419244.1:n.-61A>T
ENST00000565169.1:c.5A>T
ENST00000569170.5:c.5A>T
NM_001195794.1:c.276A>T , LRG_700t1:c.276A>T	NP_001182723.1:p.Ala92=
NM_001256819.1:c.448A>T	NP_001243748.1:p.Asn150Tyr
NM_052995.2:c.48A>T , LRG_700t2:c.48A>T	NP_443721.1:p.Ala16=
NM_174878.2:c.276A>T	NP_777367.1:p.Ala92=
NR_046380.2:n.718A>T
XR_924167.1:n.588A>T
NM_001256819.2:c.448A>T	NP_001243748.1:p.Asn150Tyr
NM_174878.3:c.276A>T MANE Select	NP_777367.1:p.Ala92=
NR_046380.3:n.446A>T