Canonical Allele Identifier: CA2635403734
Gene: TRPV3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3524066_3524067insTG , CM000679.2:g.3524066_3524067insTG GRCh38
NC_000017.10:g.3427360_3427361insTG , CM000679.1:g.3427360_3427361insTG GRCh37
NC_000017.9:g.3374110_3374111insTG NCBI36
NG_032144.2:g.38929_38930insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000576742.6:c.1743+131_1743+132insCA MANE Select ENSP00000461518.2:n.1743+131_1743+132insCA
ENST00000301365.8:c.1743+131_1743+132insCA ENSP00000301365.4:n.1743+131_1743+132insCA
ENST00000381913.8:c.1005+131_1005+132insCA
ENST00000571139.5:c.*1735+131_*1735+132insCA ENSP00000458187.1:n.*1735+131_*1735+132insCA
ENST00000572519.1:c.1743+131_1743+132insCA ENSP00000460215.1:n.1743+131_1743+132insCA
ENST00000573539.5:c.*1753+131_*1753+132insCA ENSP00000458239.1:n.*1753+131_*1753+132insCA
ENST00000576742.5:c.1743+131_1743+132insCA ENSP00000461518.1:n.1743+131_1743+132insCA
ENST00000577016.5:c.328+2787_328+2788insCA
ENST00000616411.4:c.1695+131_1695+132insCA ENSP00000483947.1:n.1695+131_1695+132insCA
NM_001258205.1:c.1743+131_1743+132insCA NP_001245134.1:n.1743+131_1743+132insCA
NM_145068.3:c.1743+131_1743+132insCA NP_659505.1:n.1743+131_1743+132insCA
XM_011523693.1:c.1577+2787_1577+2788insCA XP_011521995.1:n.1577+2787_1577+2788insCA
XM_011523694.1:c.1038+131_1038+132insCA XP_011521996.1:n.1038+131_1038+132insCA
XM_011523695.1:c.696+131_696+132insCA XP_011521997.1:n.696+131_696+132insCA
XR_934004.1:n.1817+131_1817+132insCA
NM_001258205.2:c.1743+131_1743+132insCA NP_001245134.1:n.1743+131_1743+132insCA
NM_145068.4:c.1743+131_1743+132insCA MANE Select NP_659505.1:n.1743+131_1743+132insCA