Canonical Allele Identifier: CA631707513
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs1409486191

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214441_9214442insTG , CM000681.2:g.9214441_9214442insTG GRCh38
NC_000019.9:g.9325117_9325118insTG , CM000681.1:g.9325117_9325118insTG GRCh37
NC_000019.8:g.9186117_9186118insTG NCBI36
NG_027953.1:g.5430_5431insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.396_397insCA ENSP00000493404.1:p.Thr133GlnfsTer5
ENST00000641669.1:c.396_397insCA MANE Select ENSP00000493383.1:p.Thr133GlnfsTer5
ENST00000308682.3:c.396_397insCA ENSP00000310488.2:p.Thr133GlnfsTer5
NM_001005191.2:c.396_397insCA NP_001005191.1:p.Thr133GlnfsTer5
NM_001005191.3:c.396_397insCA MANE Select NP_001005191.1:p.Thr133GlnfsTer5