Canonical Allele Identifier: CA436265386

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659499G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941712G>C , CM000665.2:g.150941712G>C	GRCh38
NC_000003.11:g.150659499G>C , CM000665.1:g.150659499G>C	GRCh37
NC_000003.10:g.152142189G>C	NCBI36
NG_009168.1:g.36288C>G , LRG_700:g.36288C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.303C>G MANE Select	ENSP00000322280.1:p.Val101=
ENST00000468836.2:c.451C>G	ENSP00000419892.2:p.His151Asp
ENST00000644099.1:c.295C>G	ENSP00000494762.1:n.295C>G
ENST00000295911.6:c.75C>G	ENSP00000295911.2:p.Val25=
ENST00000327047.5:c.303C>G	ENSP00000322280.1:p.Val101=
ENST00000328863.8:c.303C>G	ENSP00000329158.4:p.Val101=
ENST00000468836.1:c.75C>G	ENSP00000419892.1:p.Val25=
ENST00000472224.1:n.309C>G
ENST00000485607.1:c.-34C>G	ENSP00000419244.1:n.-34C>G
ENST00000565169.1:c.32C>G
ENST00000569170.5:c.32C>G
NM_001195794.1:c.303C>G , LRG_700t1:c.303C>G	NP_001182723.1:p.Val101=
NM_001256819.1:c.475C>G	NP_001243748.1:p.His159Asp
NM_052995.2:c.75C>G , LRG_700t2:c.75C>G	NP_443721.1:p.Val25=
NM_174878.2:c.303C>G	NP_777367.1:p.Val101=
NR_046380.2:n.745C>G
XR_924167.1:n.615C>G
NM_001256819.2:c.475C>G	NP_001243748.1:p.His159Asp
NM_174878.3:c.303C>G MANE Select	NP_777367.1:p.Val101=
NR_046380.3:n.473C>G