Canonical Allele Identifier: CA355011764

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690258G>C (hg19) ; chr3:g.150972471G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972471G>C , CM000665.2:g.150972471G>C	GRCh38
NC_000003.11:g.150690258G>C , CM000665.1:g.150690258G>C	GRCh37
NC_000003.10:g.152172948G>C	NCBI36
NG_009168.1:g.5529C>G , LRG_700:g.5529C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.238C>G MANE Select	ENSP00000322280.1:p.Pro80Ala
ENST00000468836.2:c.214C>G	ENSP00000419892.2:p.Pro72Ala
ENST00000644099.1:c.79C>G	ENSP00000494762.1:p.Pro27Ala
ENST00000645441.1:c.80C>G
ENST00000327047.5:c.238C>G	ENSP00000322280.1:p.Pro80Ala
ENST00000328863.8:c.238C>G	ENSP00000329158.4:p.Pro80Ala
ENST00000468836.1:c.-163C>G	ENSP00000419892.1:n.-163C>G
ENST00000472224.1:n.244C>G
NM_001195794.1:c.238C>G , LRG_700t1:c.238C>G	NP_001182723.1:p.Pro80Ala
NM_001256819.1:c.238C>G	NP_001243748.1:p.Pro80Ala
NM_174878.2:c.238C>G	NP_777367.1:p.Pro80Ala
NR_046380.2:n.529C>G
XR_924167.1:n.550C>G
NM_001256819.2:c.238C>G	NP_001243748.1:p.Pro80Ala
NM_174878.3:c.238C>G MANE Select	NP_777367.1:p.Pro80Ala
NR_046380.3:n.257C>G