Canonical Allele Identifier: CA2202634490
Gene: OR1F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3203073C= , CM000678.2:g.3203073C= GRCh38
NC_000016.9:g.3253073C= , CM000678.1:g.3253073C= GRCh37
NC_000016.8:g.3193074C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304646.3:c.-12-1162C= MANE Select ENSP00000305424.2:n.-12-1162C=
ENST00000576468.1:n.418+11736C=
ENST00000652759.1:n.424-2268C=
XM_011522506.1:c.19-1162C= XP_011520808.1:n.19-1162C=
XM_011522507.1:c.-12-1162C= XP_011520809.1:n.-12-1162C=
XM_011522508.1:c.-12-1162C= XP_011520810.1:n.-12-1162C=
XM_011522509.1:c.-406C= XP_011520811.1:n.-406C=
XM_011522506.3:c.19-1162C= XP_011520808.1:n.19-1162C=
XM_011522507.3:c.-12-1162C= XP_011520809.1:n.-12-1162C=
NM_001370639.1:c.19-1162C= NP_001357568.1:n.19-1162C=
NM_001370640.2:c.19-1162C= NP_001357569.1:n.19-1162C=
NM_001370641.1:c.-252-154C= NP_001357570.1:n.-252-154C=
NM_012360.2:c.-12-1162C= NP_036492.1:n.-12-1162C=
NM_001370640.3:c.19-1162C= NP_001357569.1:n.19-1162C=