Canonical Allele Identifier: CA2202634480
Gene: OR1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3203058G= , CM000678.2:g.3203058G= GRCh38
NC_000016.9:g.3253058G= , CM000678.1:g.3253058G= GRCh37
NC_000016.8:g.3193059G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304646.3:c.-12-1177G= MANE Select ENSP00000305424.2:n.-12-1177G=
ENST00000576468.1:n.418+11721G=
ENST00000652759.1:n.424-2283G=
XM_011522506.1:c.19-1177G= XP_011520808.1:n.19-1177G=
XM_011522507.1:c.-12-1177G= XP_011520809.1:n.-12-1177G=
XM_011522508.1:c.-12-1177G= XP_011520810.1:n.-12-1177G=
XM_011522509.1:c.-421G= XP_011520811.1:n.-421G=
XM_011522506.3:c.19-1177G= XP_011520808.1:n.19-1177G=
XM_011522507.3:c.-12-1177G= XP_011520809.1:n.-12-1177G=
NM_001370639.1:c.19-1177G= NP_001357568.1:n.19-1177G=
NM_001370640.2:c.19-1177G= NP_001357569.1:n.19-1177G=
NM_001370641.1:c.-252-169G= NP_001357570.1:n.-252-169G=
NM_012360.2:c.-12-1177G= NP_036492.1:n.-12-1177G=
NM_001370640.3:c.19-1177G= NP_001357569.1:n.19-1177G=