Canonical Allele Identifier: CA436265483

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150941736-G-A
• MyVariant Identifiers: chr3:g.150659523G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941736G>A , CM000665.2:g.150941736G>A	GRCh38
NC_000003.11:g.150659523G>A , CM000665.1:g.150659523G>A	GRCh37
NC_000003.10:g.152142213G>A	NCBI36
NG_009168.1:g.36264C>T , LRG_700:g.36264C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.279C>T MANE Select	ENSP00000322280.1:p.Ile93=
ENST00000468836.2:c.427C>T	ENSP00000419892.2:p.Pro143Ser
ENST00000644099.1:c.271C>T	ENSP00000494762.1:n.271C>T
ENST00000295911.6:c.51C>T	ENSP00000295911.2:p.Ile17=
ENST00000327047.5:c.279C>T	ENSP00000322280.1:p.Ile93=
ENST00000328863.8:c.279C>T	ENSP00000329158.4:p.Ile93=
ENST00000468836.1:c.51C>T	ENSP00000419892.1:p.Ile17=
ENST00000472224.1:n.285C>T
ENST00000485607.1:c.-58C>T	ENSP00000419244.1:n.-58C>T
ENST00000565169.1:c.8C>T
ENST00000569170.5:c.8C>T
NM_001195794.1:c.279C>T , LRG_700t1:c.279C>T	NP_001182723.1:p.Ile93=
NM_001256819.1:c.451C>T	NP_001243748.1:p.Pro151Ser
NM_052995.2:c.51C>T , LRG_700t2:c.51C>T	NP_443721.1:p.Ile17=
NM_174878.2:c.279C>T	NP_777367.1:p.Ile93=
NR_046380.2:n.721C>T
XR_924167.1:n.591C>T
NM_001256819.2:c.451C>T	NP_001243748.1:p.Pro151Ser
NM_174878.3:c.279C>T MANE Select	NP_777367.1:p.Ile93=
NR_046380.3:n.449C>T