Canonical Allele Identifier: CA497454505

Gene: TRPV3

Linked Data

• gnomAD v4: 17-3524284-G-A
• MyVariant Identifiers: chr17:g.3427578G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3524284G>A , CM000679.2:g.3524284G>A	GRCh38
NC_000017.10:g.3427578G>A , CM000679.1:g.3427578G>A	GRCh37
NC_000017.9:g.3374328G>A	NCBI36
NG_032144.2:g.38712C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576742.6:c.1657C>T MANE Select	ENSP00000461518.2:p.Leu553=
ENST00000301365.8:c.1657C>T	ENSP00000301365.4:p.Leu553=
ENST00000381913.8:c.919C>T
ENST00000571139.5:c.*1649C>T	ENSP00000458187.1:n.*1649C>T
ENST00000572519.1:c.1657C>T	ENSP00000460215.1:p.Leu553=
ENST00000573539.5:c.*1667C>T	ENSP00000458239.1:n.*1667C>T
ENST00000576742.5:c.1657C>T	ENSP00000461518.1:p.Leu553=
ENST00000577016.5:c.328+2570C>T
ENST00000616411.4:c.1609C>T	ENSP00000483947.1:p.Leu537=
NM_001258205.1:c.1657C>T	NP_001245134.1:p.Leu553=
NM_145068.3:c.1657C>T	NP_659505.1:p.Leu553=
XM_011523693.1:c.1577+2570C>T	XP_011521995.1:n.1577+2570C>T
XM_011523694.1:c.952C>T	XP_011521996.1:p.Leu318=
XM_011523695.1:c.610C>T	XP_011521997.1:p.Leu204=
XR_934004.1:n.1731C>T
NM_001258205.2:c.1657C>T	NP_001245134.1:p.Leu553=
NM_145068.4:c.1657C>T MANE Select	NP_659505.1:p.Leu553=