Canonical Allele Identifier: CA397690340
Gene: TRPV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3583409T>A , CM000679.2:g.3583409T>A GRCh38
NC_000017.10:g.3486703T>A , CM000679.1:g.3486703T>A GRCh37
NC_000017.9:g.3433452T>A NCBI36
NG_029716.1:g.31003A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000572705.2:c.1405A>T MANE Select ENSP00000459962.1:p.Thr469Ser
ENST00000650505.1:c.1405A>T ENSP00000497337.1:p.Thr469Ser
ENST00000310522.5:c.1225A>T ENSP00000311692.5:p.Thr409Ser
ENST00000399756.8:c.1405A>T ENSP00000382659.4:p.Thr469Ser
ENST00000399759.7:c.1405A>T ENSP00000382661.3:p.Thr469Ser
ENST00000425167.6:c.1438A>T ENSP00000409627.2:p.Thr480Ser
ENST00000571088.5:c.1405A>T ENSP00000461007.1:p.Thr469Ser
ENST00000572705.1:c.1405A>T ENSP00000459962.1:p.Thr469Ser
ENST00000574085.5:n.1492A>T
ENST00000576351.5:c.1375A>T ENSP00000459042.1:p.Thr459Ser
NM_018727.5:c.1405A>T NP_061197.4:p.Thr469Ser
NM_080704.3:c.1405A>T NP_542435.2:p.Thr469Ser
NM_080705.3:c.1405A>T NP_542436.2:p.Thr469Ser
NM_080706.3:c.1405A>T NP_542437.2:p.Thr469Ser
NM_080704.4:c.1405A>T MANE Select NP_542435.2:p.Thr469Ser
NM_080705.4:c.1405A>T NP_542436.2:p.Thr469Ser