Canonical Allele Identifier: CA397681891

Gene: TRPV3

Linked Data

• gnomAD v4: 17-3524296-C-A
• MyVariant Identifiers: chr17:g.3427590C>A (hg19) ; chr17:g.3524296C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3524296C>A , CM000679.2:g.3524296C>A	GRCh38
NC_000017.10:g.3427590C>A , CM000679.1:g.3427590C>A	GRCh37
NC_000017.9:g.3374340C>A	NCBI36
NG_032144.2:g.38700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576742.6:c.1645G>T MANE Select	ENSP00000461518.2:p.Ala549Ser
ENST00000301365.8:c.1645G>T	ENSP00000301365.4:p.Ala549Ser
ENST00000381913.8:c.907G>T
ENST00000571139.5:c.*1637G>T	ENSP00000458187.1:n.*1637G>T
ENST00000572519.1:c.1645G>T	ENSP00000460215.1:p.Ala549Ser
ENST00000573539.5:c.*1655G>T	ENSP00000458239.1:n.*1655G>T
ENST00000576742.5:c.1645G>T	ENSP00000461518.1:p.Ala549Ser
ENST00000577016.5:c.328+2558G>T
ENST00000616411.4:c.1597G>T	ENSP00000483947.1:p.Ala533Ser
NM_001258205.1:c.1645G>T	NP_001245134.1:p.Ala549Ser
NM_145068.3:c.1645G>T	NP_659505.1:p.Ala549Ser
XM_011523693.1:c.1577+2558G>T	XP_011521995.1:n.1577+2558G>T
XM_011523694.1:c.940G>T	XP_011521996.1:p.Ala314Ser
XM_011523695.1:c.598G>T	XP_011521997.1:p.Ala200Ser
XR_934004.1:n.1719G>T
NM_001258205.2:c.1645G>T	NP_001245134.1:p.Ala549Ser
NM_145068.4:c.1645G>T MANE Select	NP_659505.1:p.Ala549Ser