Canonical Allele Identifier: CA355012102

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690420T>C (hg19) ; chr3:g.150972633T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972633T>C , CM000665.2:g.150972633T>C	GRCh38
NC_000003.11:g.150690420T>C , CM000665.1:g.150690420T>C	GRCh37
NC_000003.10:g.152173110T>C	NCBI36
NG_009168.1:g.5367A>G , LRG_700:g.5367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.76A>G MANE Select	ENSP00000322280.1:p.Thr26Ala
ENST00000468836.2:c.52A>G	ENSP00000419892.2:p.Thr18Ala
ENST00000327047.5:c.76A>G	ENSP00000322280.1:p.Thr26Ala
ENST00000328863.8:c.76A>G	ENSP00000329158.4:p.Thr26Ala
ENST00000468836.1:c.-325A>G	ENSP00000419892.1:n.-325A>G
ENST00000472224.1:n.82A>G
NM_001195794.1:c.76A>G , LRG_700t1:c.76A>G	NP_001182723.1:p.Thr26Ala
NM_001256819.1:c.76A>G	NP_001243748.1:p.Thr26Ala
NM_174878.2:c.76A>G	NP_777367.1:p.Thr26Ala
NR_046380.2:n.367A>G
XR_924167.1:n.388A>G
NM_001256819.2:c.76A>G	NP_001243748.1:p.Thr26Ala
NM_174878.3:c.76A>G MANE Select	NP_777367.1:p.Thr26Ala
NR_046380.3:n.95A>G