Canonical Allele Identifier: CA2243937756

Gene: TRPV1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3574518C= , CM000679.2:g.3574518C=	GRCh38
NC_000017.10:g.3477812C= , CM000679.1:g.3477812C=	GRCh37
NC_000017.9:g.3424561C=	NCBI36
NG_029716.1:g.39894G=

Transcript Alleles

HGVS	Amino-acid Change
NM_080704.4:c.1781-563G= MANE Select	NP_542435.2:n.1781-563G=
ENST00000572705.2:c.1781-563G= MANE Select	ENSP00000459962.1:n.1781-563G=
NM_018727.5:c.1781-563G=	NP_061197.4:n.1781-563G=
NM_080704.3:c.1781-563G=	NP_542435.2:n.1781-563G=
NM_080705.3:c.1781-563G=	NP_542436.2:n.1781-563G=
NM_080705.4:c.1781-563G=	NP_542436.2:n.1781-563G=
NM_080706.3:c.1781-563G=	NP_542437.2:n.1781-563G=
ENST00000310522.5:c.1601-563G=	ENSP00000311692.5:n.1601-563G=
ENST00000399756.8:c.1781-563G=	ENSP00000382659.4:n.1781-563G=
ENST00000399759.7:c.1781-563G=	ENSP00000382661.3:n.1781-563G=
ENST00000425167.6:c.1814-563G=	ENSP00000409627.2:n.1814-563G=
ENST00000570742.1:n.359-563G=
ENST00000571088.5:c.1781-563G=	ENSP00000461007.1:n.1781-563G=
ENST00000572705.1:c.1781-563G=	ENSP00000459962.1:n.1781-563G=
ENST00000574085.5:n.1868-563G=
ENST00000576351.5:c.1751-563G=	ENSP00000459042.1:n.1751-563G=
ENST00000650505.1:c.*262-563G=	ENSP00000497337.1:n.*262-563G=