Canonical Allele Identifier: CA354956121

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659531T>C (hg19) ; chr3:g.150941744T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941744T>C , CM000665.2:g.150941744T>C	GRCh38
NC_000003.11:g.150659531T>C , CM000665.1:g.150659531T>C	GRCh37
NC_000003.10:g.152142221T>C	NCBI36
NG_009168.1:g.36256A>G , LRG_700:g.36256A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.271A>G MANE Select	ENSP00000322280.1:p.Lys91Glu
ENST00000468836.2:c.419A>G	ENSP00000419892.2:p.Gln140Arg
ENST00000644099.1:c.263A>G	ENSP00000494762.1:n.263A>G
ENST00000295911.6:c.43A>G	ENSP00000295911.2:p.Lys15Glu
ENST00000327047.5:c.271A>G	ENSP00000322280.1:p.Lys91Glu
ENST00000328863.8:c.271A>G	ENSP00000329158.4:p.Lys91Glu
ENST00000468836.1:c.43A>G	ENSP00000419892.1:p.Lys15Glu
ENST00000472224.1:n.277A>G
ENST00000485607.1:c.-66A>G	ENSP00000419244.1:n.-66A>G
NM_001195794.1:c.271A>G , LRG_700t1:c.271A>G	NP_001182723.1:p.Lys91Glu
NM_001256819.1:c.443A>G	NP_001243748.1:p.Gln148Arg
NM_052995.2:c.43A>G , LRG_700t2:c.43A>G	NP_443721.1:p.Lys15Glu
NM_174878.2:c.271A>G	NP_777367.1:p.Lys91Glu
NR_046380.2:n.713A>G
XR_924167.1:n.583A>G
NM_001256819.2:c.443A>G	NP_001243748.1:p.Gln148Arg
NM_174878.3:c.271A>G MANE Select	NP_777367.1:p.Lys91Glu
NR_046380.3:n.441A>G