Canonical Allele Identifier: CA728329665

Gene: TRPV3

Linked Data

• dbSNP Id: rs1449458275
• gnomAD v3: 17-3518487-A-G
• gnomAD v4: 17-3518487-A-G
• MyVariant Identifiers: chr17:g.3421781A>G (hg19) ; chr17:g.3518487A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3518487A>G , CM000679.2:g.3518487A>G	GRCh38
NC_000017.10:g.3421781A>G , CM000679.1:g.3421781A>G	GRCh37
NC_000017.9:g.3368531A>G	NCBI36
NG_032144.2:g.44509T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000576742.6:c.2085+89T>C MANE Select	ENSP00000461518.2:n.2085+89T>C
ENST00000301365.8:c.2085+89T>C	ENSP00000301365.4:n.2085+89T>C
ENST00000381913.8:c.1347+89T>C
ENST00000571139.5:c.*2077+89T>C	ENSP00000458187.1:n.*2077+89T>C
ENST00000572519.1:c.2085+89T>C	ENSP00000460215.1:n.2085+89T>C
ENST00000573539.5:c.*2095+89T>C	ENSP00000458239.1:n.*2095+89T>C
ENST00000576742.5:c.2085+89T>C	ENSP00000461518.1:n.2085+89T>C
ENST00000577016.5:c.603+89T>C
ENST00000616411.4:c.2037+89T>C	ENSP00000483947.1:n.2037+89T>C
NM_001258205.1:c.2085+89T>C	NP_001245134.1:n.2085+89T>C
NM_145068.3:c.2085+89T>C	NP_659505.1:n.2085+89T>C
XM_011523694.1:c.1380+89T>C	XP_011521996.1:n.1380+89T>C
XM_011523695.1:c.1038+89T>C	XP_011521997.1:n.1038+89T>C
XR_934004.1:n.2159+89T>C
NM_001258205.2:c.2085+89T>C	NP_001245134.1:n.2085+89T>C
NM_145068.4:c.2085+89T>C MANE Select	NP_659505.1:n.2085+89T>C