Canonical Allele Identifier: CA397681792
Gene: TRPV3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3524247T>G , CM000679.2:g.3524247T>G GRCh38
NC_000017.10:g.3427541T>G , CM000679.1:g.3427541T>G GRCh37
NC_000017.9:g.3374291T>G NCBI36
NG_032144.2:g.38749A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000576742.6:c.1694A>C MANE Select ENSP00000461518.2:p.Tyr565Ser
ENST00000301365.8:c.1694A>C ENSP00000301365.4:p.Tyr565Ser
ENST00000381913.8:c.956A>C
ENST00000571139.5:c.*1686A>C ENSP00000458187.1:n.*1686A>C
ENST00000572519.1:c.1694A>C ENSP00000460215.1:p.Tyr565Ser
ENST00000573539.5:c.*1704A>C ENSP00000458239.1:n.*1704A>C
ENST00000576742.5:c.1694A>C ENSP00000461518.1:p.Tyr565Ser
ENST00000577016.5:c.328+2607A>C
ENST00000616411.4:c.1646A>C ENSP00000483947.1:p.Tyr549Ser
NM_001258205.1:c.1694A>C NP_001245134.1:p.Tyr565Ser
NM_145068.3:c.1694A>C NP_659505.1:p.Tyr565Ser
XM_011523693.1:c.1577+2607A>C XP_011521995.1:n.1577+2607A>C
XM_011523694.1:c.989A>C XP_011521996.1:p.Tyr330Ser
XM_011523695.1:c.647A>C XP_011521997.1:p.Tyr216Ser
XR_934004.1:n.1768A>C
NM_001258205.2:c.1694A>C NP_001245134.1:p.Tyr565Ser
NM_145068.4:c.1694A>C MANE Select NP_659505.1:p.Tyr565Ser