Canonical Allele Identifier: CA1950353263
Gene: OR10A2 HGNC NCBI
OR2AG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6868428_6868438delinsTTCTCTATCCC , CM000673.2:g.6868428_6868438delinsTTCTCTATCCC GRCh38
NC_000011.9:g.6889659_6889669delinsTTCTCTATCCC , CM000673.1:g.6889659_6889669delinsTTCTCTATCCC GRCh37
NC_000011.8:g.6846235_6846245delinsTTCTCTATCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641461.1:c.-132-1195_-132-1185delinsTTCTCTATCCC (OR10A2) MANE Select ENSP00000493131.1:n.-132-1195_-132-1185delinsTTCTCTATCCC
XM_011520058.1:c.-436+29655_-436+29665delinsGGGATAGAGAA (OR2AG2) XP_011518360.1:n.-436+29655_-436+29665delinsGGGATAGAGAA
XM_011520059.1:c.-436+29655_-436+29665delinsGGGATAGAGAA (OR2AG2) XP_011518361.1:n.-436+29655_-436+29665delinsGGGATAGAGAA
XM_011520060.1:c.-436+29655_-436+29665delinsGGGATAGAGAA (OR2AG2) XP_011518362.1:n.-436+29655_-436+29665delinsGGGATAGAGAA
XM_011520061.1:c.-436+56060_-436+56070delinsGGGATAGAGAA (OR2AG2) XP_011518363.1:n.-436+56060_-436+56070delinsGGGATAGAGAA
NM_001004460.2:c.-132-1195_-132-1185delinsTTCTCTATCCC (OR10A2) MANE Select NP_001004460.1:n.-132-1195_-132-1185delinsTTCTCTATCCC