Canonical Allele Identifier: CA13371660

Gene: TRIM5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5666794G>C , CM000673.2:g.5666794G>C	GRCh38
NC_000011.9:g.5688024G>C , CM000673.1:g.5688024G>C	GRCh37
NC_000011.8:g.5644600G>C	NCBI36
NG_029122.1:g.23316C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682968.1:c.767+895C>G	ENSP00000506742.1:n.767+895C>G
ENST00000684417.1:n.1190-713C>G
ENST00000684655.1:c.768-713C>G	ENSP00000507420.1:n.768-713C>G
ENST00000380034.8:c.768-713C>G MANE Select	ENSP00000369373.3:n.768-713C>G
ENST00000380259.7:c.231+11410C>G	ENSP00000369609.3:n.231+11410C>G
ENST00000642298.1:n.24-713C>G
ENST00000380027.5:c.768-713C>G	ENSP00000369366.1:n.768-713C>G
ENST00000380034.7:c.768-713C>G	ENSP00000369373.3:n.768-713C>G
ENST00000396847.7:c.768-713C>G	ENSP00000380058.3:n.768-713C>G
ENST00000433961.5:c.745-713C>G	ENSP00000393052.1:n.745-713C>G
ENST00000438025.5:c.397+895C>G
ENST00000465634.5:n.401-713C>G
ENST00000483835.5:n.448-713C>G
ENST00000492086.5:n.299-713C>G
NM_033034.2:c.768-713C>G	NP_149023.2:n.768-713C>G
NM_033092.2:c.768-713C>G	NP_149083.2:n.768-713C>G
NM_033093.2:c.768-713C>G	NP_149084.2:n.768-713C>G
XM_005253183.1:c.768-713C>G	XP_005253240.1:n.768-713C>G
XM_005253184.1:c.768-713C>G	XP_005253241.1:n.768-713C>G
XM_006718358.1:c.767+895C>G	XP_006718421.1:n.767+895C>G
XM_011520424.1:c.768-713C>G	XP_011518726.1:n.768-713C>G
XM_011520425.1:c.767+895C>G	XP_011518727.1:n.767+895C>G
XM_011520426.1:c.767+895C>G	XP_011518728.1:n.767+895C>G
XM_011520427.1:c.745-713C>G	XP_011518729.1:n.745-713C>G
XR_930919.1:n.1056+895C>G
XR_930920.1:n.1034-713C>G
XR_930921.1:n.1034-713C>G
XM_005253183.3:c.768-713C>G	XP_005253240.1:n.768-713C>G
XM_005253184.3:c.768-713C>G	XP_005253241.1:n.768-713C>G
XM_006718358.3:c.767+895C>G	XP_006718421.1:n.767+895C>G
XM_011520426.3:c.767+895C>G	XP_011518728.1:n.767+895C>G
XM_011520427.2:c.745-713C>G	XP_011518729.1:n.745-713C>G
XM_017018461.2:c.767+895C>G	XP_016873950.1:n.767+895C>G
XM_017018462.2:c.768-713C>G	XP_016873951.1:n.768-713C>G
XM_017018463.2:c.767+895C>G	XP_016873952.1:n.767+895C>G
XR_001748014.2:n.1046-713C>G
XR_001748015.2:n.1045+895C>G
XR_001748016.2:n.899-713C>G
XR_001748017.2:n.1023-713C>G
XR_001748018.2:n.1022+11410C>G
XR_930920.3:n.1023-713C>G
XR_930921.2:n.1023-713C>G
NM_033034.3:c.768-713C>G MANE Select	NP_149023.2:n.768-713C>G
NM_033092.3:c.768-713C>G	NP_149083.2:n.768-713C>G
NM_033093.3:c.768-713C>G	NP_149084.2:n.768-713C>G
NM_033092.4:c.768-713C>G	NP_149083.2:n.768-713C>G
NM_033093.4:c.768-713C>G	NP_149084.2:n.768-713C>G