Canonical Allele Identifier: CA5992617
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs754932155
ExAC: 11:55578958 T / TGCACC
gnomAD v2: 11-55578958-T-TGCACC
gnomAD v3: 11-55811482-T-TGCACC
gnomAD v4: 11-55811482-T-TGCACC
MyVariant Identifiers: chr11:g.55578958_55578959insGCACC (hg19) chr11:g.55811482_55811483insGCACC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811483_55811487dup , CM000673.2:g.55811483_55811487dup GRCh38
NC_000011.9:g.55578959_55578963dup , CM000673.1:g.55578959_55578963dup GRCh37
NC_000011.8:g.55335535_55335539dup NCBI36
NG_052620.1:g.5117_5121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.17_21dup MANE Select ENSP00000485319.1:p.Thr8AlafsTer18
ENST00000333973.3:c.17_21dup ENSP00000335529.2:p.Thr8AlafsTer18
ENST00000623450.1:c.17_21dup ENSP00000485509.1:p.Thr8AlafsTer18
ENST00000625203.1:c.17_21dup ENSP00000485319.1:p.Thr8AlafsTer18
NM_001004738.1:c.17_21dup NP_001004738.1:p.Thr8AlafsTer18
NM_001004738.2:c.17_21dup MANE Select NP_001004738.1:p.Thr8AlafsTer18
Search 100 bp 5'
Search 100 bp 3'