Canonical Allele Identifier: CA397681776

Gene: TRPV3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3524238C>A , CM000679.2:g.3524238C>A	GRCh38
NC_000017.10:g.3427532C>A , CM000679.1:g.3427532C>A	GRCh37
NC_000017.9:g.3374282C>A	NCBI36
NG_032144.2:g.38758G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576742.6:c.1703G>T MANE Select	ENSP00000461518.2:p.Gly568Val
ENST00000301365.8:c.1703G>T	ENSP00000301365.4:p.Gly568Val
ENST00000381913.8:c.965G>T
ENST00000571139.5:c.*1695G>T	ENSP00000458187.1:n.*1695G>T
ENST00000572519.1:c.1703G>T	ENSP00000460215.1:p.Gly568Val
ENST00000573539.5:c.*1713G>T	ENSP00000458239.1:n.*1713G>T
ENST00000576742.5:c.1703G>T	ENSP00000461518.1:p.Gly568Val
ENST00000577016.5:c.328+2616G>T
ENST00000616411.4:c.1655G>T	ENSP00000483947.1:p.Gly552Val
NM_001258205.1:c.1703G>T	NP_001245134.1:p.Gly568Val
NM_145068.3:c.1703G>T	NP_659505.1:p.Gly568Val
XM_011523693.1:c.1577+2616G>T	XP_011521995.1:n.1577+2616G>T
XM_011523694.1:c.998G>T	XP_011521996.1:p.Gly333Val
XM_011523695.1:c.656G>T	XP_011521997.1:p.Gly219Val
XR_934004.1:n.1777G>T
NM_001258205.2:c.1703G>T	NP_001245134.1:p.Gly568Val
NM_145068.4:c.1703G>T MANE Select	NP_659505.1:p.Gly568Val