Canonical Allele Identifier: CA363965943
Gene: CLIC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.45955171C>A , CM000668.2:g.45955171C>A GRCh38
NC_000006.11:g.45922908C>A , CM000668.1:g.45922908C>A GRCh37
NC_000006.10:g.46030886C>A NCBI36
NG_031965.1:g.130178G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000185206.12:c.614G>T ENSP00000185206.6:p.Gly205Val
ENST00000339561.12:c.137G>T MANE Select ENSP00000344165.6:p.Gly46Val
ENST00000544153.3:c.137G>T ENSP00000439195.1:p.Gly46Val
ENST00000642250.1:c.137G>T ENSP00000496359.1:p.Gly46Val
ENST00000644324.1:c.137G>T ENSP00000495186.1:p.Gly46Val
ENST00000644878.1:c.137G>T ENSP00000493894.1:p.Gly46Val
ENST00000672327.1:c.137G>T ENSP00000500472.1:p.Gly46Val
ENST00000185206.10:c.614G>T ENSP00000185206.6:p.Gly205Val
ENST00000339561.10:c.137G>T ENSP00000344165.6:p.Gly46Val
ENST00000544153.2:c.137G>T ENSP00000439195.1:p.Gly46Val
NM_001114086.1:c.614G>T NP_001107558.1:p.Gly205Val
NM_001256023.1:c.137G>T NP_001242952.1:p.Gly46Val
NM_016929.4:c.137G>T NP_058625.2:p.Gly46Val
XM_011514692.1:c.614G>T XP_011512994.1:p.Gly205Val
XM_011514693.1:c.614G>T XP_011512995.1:p.Gly205Val
XM_011514694.1:c.614G>T XP_011512996.1:p.Gly205Val
XM_011514695.1:c.20G>T XP_011512997.1:p.Gly7Val
XR_926257.1:n.659G>T
XR_926258.1:n.659G>T
XR_926259.1:n.659G>T
XM_011514692.3:c.614G>T XP_011512994.1:p.Gly205Val
XM_011514694.3:c.614G>T XP_011512996.1:p.Gly205Val
XM_017010953.1:c.614G>T XP_016866442.1:p.Gly205Val
XR_926258.3:n.727G>T
NM_001114086.2:c.614G>T NP_001107558.1:p.Gly205Val
NM_001370649.1:c.20G>T NP_001357578.1:p.Gly7Val
NM_001370650.1:c.614G>T NP_001357579.1:p.Gly205Val
NM_016929.5:c.137G>T MANE Select NP_058625.2:p.Gly46Val
NM_001256023.2:c.137G>T NP_001242952.1:p.Gly46Val