Canonical Allele Identifier: CA436402924

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690265T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972478T>G , CM000665.2:g.150972478T>G	GRCh38
NC_000003.11:g.150690265T>G , CM000665.1:g.150690265T>G	GRCh37
NC_000003.10:g.152172955T>G	NCBI36
NG_009168.1:g.5522A>C , LRG_700:g.5522A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.231A>C MANE Select	ENSP00000322280.1:p.Gly77=
ENST00000468836.2:c.207A>C	ENSP00000419892.2:p.Gly69=
ENST00000644099.1:c.72A>C	ENSP00000494762.1:p.Gly24=
ENST00000645441.1:c.73A>C
ENST00000327047.5:c.231A>C	ENSP00000322280.1:p.Gly77=
ENST00000328863.8:c.231A>C	ENSP00000329158.4:p.Gly77=
ENST00000468836.1:c.-170A>C	ENSP00000419892.1:n.-170A>C
ENST00000472224.1:n.237A>C
NM_001195794.1:c.231A>C , LRG_700t1:c.231A>C	NP_001182723.1:p.Gly77=
NM_001256819.1:c.231A>C	NP_001243748.1:p.Gly77=
NM_174878.2:c.231A>C	NP_777367.1:p.Gly77=
NR_046380.2:n.522A>C
XR_924167.1:n.543A>C
NM_001256819.2:c.231A>C	NP_001243748.1:p.Gly77=
NM_174878.3:c.231A>C MANE Select	NP_777367.1:p.Gly77=
NR_046380.3:n.250A>C