Canonical Allele Identifier: CA2580604989

Gene: OR1F1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3203133A>T , CM000678.2:g.3203133A>T	GRCh38
NC_000016.9:g.3253133A>T , CM000678.1:g.3253133A>T	GRCh37
NC_000016.8:g.3193134A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000304646.3:c.-12-1102A>T MANE Select	ENSP00000305424.2:n.-12-1102A>T
ENST00000576468.1:n.418+11796A>T
ENST00000652759.1:n.424-2208A>T
XM_011522506.1:c.19-1102A>T	XP_011520808.1:n.19-1102A>T
XM_011522507.1:c.-12-1102A>T	XP_011520809.1:n.-12-1102A>T
XM_011522508.1:c.-12-1102A>T	XP_011520810.1:n.-12-1102A>T
XM_011522509.1:c.-346A>T	XP_011520811.1:n.-346A>T
XM_011522506.3:c.19-1102A>T	XP_011520808.1:n.19-1102A>T
XM_011522507.3:c.-12-1102A>T	XP_011520809.1:n.-12-1102A>T
NM_001370639.1:c.19-1102A>T	NP_001357568.1:n.19-1102A>T
NM_001370640.2:c.19-1102A>T	NP_001357569.1:n.19-1102A>T
NM_001370641.1:c.-252-94A>T	NP_001357570.1:n.-252-94A>T
NM_012360.2:c.-12-1102A>T	NP_036492.1:n.-12-1102A>T
NM_001370640.3:c.19-1102A>T	NP_001357569.1:n.19-1102A>T