Canonical Allele Identifier: CA436265497

Gene: CLRN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.276A>C MANE Select	ENSP00000322280.1:p.Ala92=
ENST00000468836.2:c.424A>C	ENSP00000419892.2:p.Asn142His
ENST00000644099.1:c.268A>C	ENSP00000494762.1:n.268A>C
ENST00000295911.6:c.48A>C	ENSP00000295911.2:p.Ala16=
ENST00000327047.5:c.276A>C	ENSP00000322280.1:p.Ala92=
ENST00000328863.8:c.276A>C	ENSP00000329158.4:p.Ala92=
ENST00000468836.1:c.48A>C	ENSP00000419892.1:p.Ala16=
ENST00000472224.1:n.282A>C
ENST00000485607.1:c.-61A>C	ENSP00000419244.1:n.-61A>C
ENST00000565169.1:c.5A>C
ENST00000569170.5:c.5A>C
NM_001195794.1:c.276A>C , LRG_700t1:c.276A>C	NP_001182723.1:p.Ala92=
NM_001256819.1:c.448A>C	NP_001243748.1:p.Asn150His
NM_052995.2:c.48A>C , LRG_700t2:c.48A>C	NP_443721.1:p.Ala16=
NM_174878.2:c.276A>C	NP_777367.1:p.Ala92=
NR_046380.2:n.718A>C
XR_924167.1:n.588A>C
NM_001256819.2:c.448A>C	NP_001243748.1:p.Asn150His
NM_174878.3:c.276A>C MANE Select	NP_777367.1:p.Ala92=
NR_046380.3:n.446A>C