Canonical Allele Identifier: CA397681947
Gene: TRPV3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3524321G>T , CM000679.2:g.3524321G>T GRCh38
NC_000017.10:g.3427615G>T , CM000679.1:g.3427615G>T GRCh37
NC_000017.9:g.3374365G>T NCBI36
NG_032144.2:g.38675C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000576742.6:c.1620C>A MANE Select ENSP00000461518.2:p.Tyr540Ter
ENST00000301365.8:c.1620C>A ENSP00000301365.4:p.Tyr540Ter
ENST00000381913.8:c.899-17C>A
ENST00000571139.5:c.*1612C>A ENSP00000458187.1:n.*1612C>A
ENST00000572519.1:c.1620C>A ENSP00000460215.1:p.Tyr540Ter
ENST00000573539.5:c.*1647-17C>A ENSP00000458239.1:n.*1647-17C>A
ENST00000576742.5:c.1620C>A ENSP00000461518.1:p.Tyr540Ter
ENST00000577016.5:c.328+2533C>A
ENST00000616411.4:c.1572C>A ENSP00000483947.1:p.Tyr524Ter
NM_001258205.1:c.1620C>A NP_001245134.1:p.Tyr540Ter
NM_145068.3:c.1620C>A NP_659505.1:p.Tyr540Ter
XM_011523693.1:c.1577+2533C>A XP_011521995.1:n.1577+2533C>A
XM_011523694.1:c.915C>A XP_011521996.1:p.Tyr305Ter
XM_011523695.1:c.573C>A XP_011521997.1:p.Tyr191Ter
XR_934004.1:n.1711-17C>A
NM_001258205.2:c.1620C>A NP_001245134.1:p.Tyr540Ter
NM_145068.4:c.1620C>A MANE Select NP_659505.1:p.Tyr540Ter