Canonical Allele Identifier: CA397681790
Gene: TRPV3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3524246A>C , CM000679.2:g.3524246A>C GRCh38
NC_000017.10:g.3427540A>C , CM000679.1:g.3427540A>C GRCh37
NC_000017.9:g.3374290A>C NCBI36
NG_032144.2:g.38750T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000576742.6:c.1695T>G MANE Select ENSP00000461518.2:p.Tyr565Ter
ENST00000301365.8:c.1695T>G ENSP00000301365.4:p.Tyr565Ter
ENST00000381913.8:c.957T>G
ENST00000571139.5:c.*1687T>G ENSP00000458187.1:n.*1687T>G
ENST00000572519.1:c.1695T>G ENSP00000460215.1:p.Tyr565Ter
ENST00000573539.5:c.*1705T>G ENSP00000458239.1:n.*1705T>G
ENST00000576742.5:c.1695T>G ENSP00000461518.1:p.Tyr565Ter
ENST00000577016.5:c.328+2608T>G
ENST00000616411.4:c.1647T>G ENSP00000483947.1:p.Tyr549Ter
NM_001258205.1:c.1695T>G NP_001245134.1:p.Tyr565Ter
NM_145068.3:c.1695T>G NP_659505.1:p.Tyr565Ter
XM_011523693.1:c.1577+2608T>G XP_011521995.1:n.1577+2608T>G
XM_011523694.1:c.990T>G XP_011521996.1:p.Tyr330Ter
XM_011523695.1:c.648T>G XP_011521997.1:p.Tyr216Ter
XR_934004.1:n.1769T>G
NM_001258205.2:c.1695T>G NP_001245134.1:p.Tyr565Ter
NM_145068.4:c.1695T>G MANE Select NP_659505.1:p.Tyr565Ter