Canonical Allele Identifier: CA2243942624

Gene: TRPV1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3583408G= , CM000679.2:g.3583408G=	GRCh38
NC_000017.10:g.3486702G= , CM000679.1:g.3486702G=	GRCh37
NC_000017.9:g.3433451G=	NCBI36
NG_029716.1:g.31004C=

Transcript Alleles

HGVS	Amino-acid Change
NM_080704.4:c.1406C= MANE Select	NP_542435.2:p.Thr469=
ENST00000572705.2:c.1406C= MANE Select	ENSP00000459962.1:p.Thr469=
NM_018727.5:c.1406C=	NP_061197.4:p.Thr469=
NM_080704.3:c.1406C=	NP_542435.2:p.Thr469=
NM_080705.3:c.1406C=	NP_542436.2:p.Thr469=
NM_080705.4:c.1406C=	NP_542436.2:p.Thr469=
NM_080706.3:c.1406C=	NP_542437.2:p.Thr469=
ENST00000310522.5:c.1226C=	ENSP00000311692.5:p.Thr409=
ENST00000399756.8:c.1406C=	ENSP00000382659.4:p.Thr469=
ENST00000399759.7:c.1406C=	ENSP00000382661.3:p.Thr469=
ENST00000425167.6:c.1439C=	ENSP00000409627.2:p.Thr480=
ENST00000571088.5:c.1406C=	ENSP00000461007.1:p.Thr469=
ENST00000572705.1:c.1406C=	ENSP00000459962.1:p.Thr469=
ENST00000574085.5:n.1493C=
ENST00000576351.5:c.1376C=	ENSP00000459042.1:p.Thr459=
ENST00000650505.1:c.1406C=	ENSP00000497337.1:p.Thr469=