Canonical Allele Identifier: CA682736949

Gene: OLR1

Linked Data

• dbSNP Id: rs1476860510
• gnomAD v4: 12-10159624-TA-T
• MyVariant Identifiers: chr12:g.10312224del (hg19) ; chr12:g.10159625del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159629del , CM000674.2:g.10159629del	GRCh38
NC_000012.11:g.10312228del , CM000674.1:g.10312228del	GRCh37
NC_000012.10:g.10203495del	NCBI36
NG_016743.1:g.17567del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*255del MANE Select	ENSP00000309124.3:n.*255del
ENST00000309539.7:c.*255del	ENSP00000309124.3:n.*255del
ENST00000543993.5:c.*391del	ENSP00000445085.1:n.*391del
ENST00000544577.5:c.*255del	ENSP00000444457.1:n.*255del
ENST00000545927.5:c.*391del	ENSP00000439251.1:n.*391del
NM_001172632.1:c.*391del	NP_001166103.1:n.*391del
NM_001172633.1:c.*391del	NP_001166104.1:n.*391del
NM_002543.3:c.*255del	NP_002534.1:n.*255del
XM_011520682.1:c.*255del	XP_011518984.1:n.*255del
XM_011520683.1:c.*407del	XP_011518985.1:n.*407del
NM_002543.4:c.*255del MANE Select	NP_002534.1:n.*255del
NM_001172632.2:c.*391del	NP_001166103.1:n.*391del
NM_001172633.2:c.*391del	NP_001166104.1:n.*391del