Canonical Allele Identifier: CA2202634478
Gene: OR1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3203057A= , CM000678.2:g.3203057A= GRCh38
NC_000016.9:g.3253057A= , CM000678.1:g.3253057A= GRCh37
NC_000016.8:g.3193058A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304646.3:c.-12-1178A= MANE Select ENSP00000305424.2:n.-12-1178A=
ENST00000576468.1:n.418+11720A=
ENST00000652759.1:n.424-2284A=
XM_011522506.1:c.19-1178A= XP_011520808.1:n.19-1178A=
XM_011522507.1:c.-12-1178A= XP_011520809.1:n.-12-1178A=
XM_011522508.1:c.-12-1178A= XP_011520810.1:n.-12-1178A=
XM_011522509.1:c.-422A= XP_011520811.1:n.-422A=
XM_011522506.3:c.19-1178A= XP_011520808.1:n.19-1178A=
XM_011522507.3:c.-12-1178A= XP_011520809.1:n.-12-1178A=
NM_001370639.1:c.19-1178A= NP_001357568.1:n.19-1178A=
NM_001370640.2:c.19-1178A= NP_001357569.1:n.19-1178A=
NM_001370641.1:c.-252-170A= NP_001357570.1:n.-252-170A=
NM_012360.2:c.-12-1178A= NP_036492.1:n.-12-1178A=
NM_001370640.3:c.19-1178A= NP_001357569.1:n.19-1178A=