Canonical Allele Identifier: CA397681941

Gene: TRPV3

Linked Data

• MyVariant Identifiers: chr17:g.3427612C>G (hg19) ; chr17:g.3524318C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3524318C>G , CM000679.2:g.3524318C>G	GRCh38
NC_000017.10:g.3427612C>G , CM000679.1:g.3427612C>G	GRCh37
NC_000017.9:g.3374362C>G	NCBI36
NG_032144.2:g.38678G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576742.6:c.1623G>C MANE Select	ENSP00000461518.2:p.Leu541Phe
ENST00000301365.8:c.1623G>C	ENSP00000301365.4:p.Leu541Phe
ENST00000381913.8:c.899-14G>C
ENST00000571139.5:c.*1615G>C	ENSP00000458187.1:n.*1615G>C
ENST00000572519.1:c.1623G>C	ENSP00000460215.1:p.Leu541Phe
ENST00000573539.5:c.*1647-14G>C	ENSP00000458239.1:n.*1647-14G>C
ENST00000576742.5:c.1623G>C	ENSP00000461518.1:p.Leu541Phe
ENST00000577016.5:c.328+2536G>C
ENST00000616411.4:c.1575G>C	ENSP00000483947.1:p.Leu525Phe
NM_001258205.1:c.1623G>C	NP_001245134.1:p.Leu541Phe
NM_145068.3:c.1623G>C	NP_659505.1:p.Leu541Phe
XM_011523693.1:c.1577+2536G>C	XP_011521995.1:n.1577+2536G>C
XM_011523694.1:c.918G>C	XP_011521996.1:p.Leu306Phe
XM_011523695.1:c.576G>C	XP_011521997.1:p.Leu192Phe
XR_934004.1:n.1711-14G>C
NM_001258205.2:c.1623G>C	NP_001245134.1:p.Leu541Phe
NM_145068.4:c.1623G>C MANE Select	NP_659505.1:p.Leu541Phe