Canonical Allele Identifier: CA2243936229

Gene: TRPV1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3571724A= , CM000679.2:g.3571724A=	GRCh38
NC_000017.10:g.3475018A= , CM000679.1:g.3475018A=	GRCh37
NC_000017.9:g.3421768A=	NCBI36
NG_029716.1:g.42688T=

Transcript Alleles

HGVS	Amino-acid Change
NM_080704.4:c.2232-85T= MANE Select	NP_542435.2:n.2232-85T=
ENST00000572705.2:c.2232-85T= MANE Select	ENSP00000459962.1:n.2232-85T=
NM_018727.5:c.2232-85T=	NP_061197.4:n.2232-85T=
NM_080704.3:c.2232-85T=	NP_542435.2:n.2232-85T=
NM_080705.3:c.2232-85T=	NP_542436.2:n.2232-85T=
NM_080705.4:c.2232-85T=	NP_542436.2:n.2232-85T=
NM_080706.3:c.2232-85T=	NP_542437.2:n.2232-85T=
ENST00000310522.5:c.2052-85T=	ENSP00000311692.5:n.2052-85T=
ENST00000399756.8:c.2232-85T=	ENSP00000382659.4:n.2232-85T=
ENST00000399759.7:c.2232-85T=	ENSP00000382661.3:n.2232-85T=
ENST00000425167.6:c.2265-85T=	ENSP00000409627.2:n.2265-85T=
ENST00000571088.5:c.2232-85T=	ENSP00000461007.1:n.2232-85T=
ENST00000572705.1:c.2232-85T=	ENSP00000459962.1:n.2232-85T=
ENST00000574085.5:n.2319-85T=
ENST00000576351.5:c.2202-85T=	ENSP00000459042.1:n.2202-85T=
ENST00000650505.1:c.*713-85T=	ENSP00000497337.1:n.*713-85T=