Canonical Allele Identifier: CA2678981845

Gene: CLIC5

Linked Data

• gnomAD v4: 6-45955376-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45955376G>A , CM000668.2:g.45955376G>A	GRCh38
NC_000006.11:g.45923113G>A , CM000668.1:g.45923113G>A	GRCh37
NC_000006.10:g.46031091G>A	NCBI36
NG_031965.1:g.129973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000185206.12:c.541-132C>T	ENSP00000185206.6:n.541-132C>T
ENST00000339561.12:c.64-132C>T MANE Select	ENSP00000344165.6:n.64-132C>T
ENST00000544153.3:c.64-132C>T	ENSP00000439195.1:n.64-132C>T
ENST00000642250.1:c.64-132C>T	ENSP00000496359.1:n.64-132C>T
ENST00000644324.1:c.64-132C>T	ENSP00000495186.1:n.64-132C>T
ENST00000644878.1:c.64-132C>T	ENSP00000493894.1:n.64-132C>T
ENST00000672327.1:c.64-132C>T	ENSP00000500472.1:n.64-132C>T
ENST00000185206.10:c.541-132C>T	ENSP00000185206.6:n.541-132C>T
ENST00000339561.10:c.64-132C>T	ENSP00000344165.6:n.64-132C>T
ENST00000544153.2:c.64-132C>T	ENSP00000439195.1:n.64-132C>T
NM_001114086.1:c.541-132C>T	NP_001107558.1:n.541-132C>T
NM_001256023.1:c.64-132C>T	NP_001242952.1:n.64-132C>T
NM_016929.4:c.64-132C>T	NP_058625.2:n.64-132C>T
XM_011514692.1:c.541-132C>T	XP_011512994.1:n.541-132C>T
XM_011514693.1:c.541-132C>T	XP_011512995.1:n.541-132C>T
XM_011514694.1:c.541-132C>T	XP_011512996.1:n.541-132C>T
XM_011514695.1:c.-54-132C>T	XP_011512997.1:n.-54-132C>T
XR_926257.1:n.586-132C>T
XR_926258.1:n.586-132C>T
XR_926259.1:n.586-132C>T
XM_011514692.3:c.541-132C>T	XP_011512994.1:n.541-132C>T
XM_011514694.3:c.541-132C>T	XP_011512996.1:n.541-132C>T
XM_017010953.1:c.541-132C>T	XP_016866442.1:n.541-132C>T
XR_926258.3:n.654-132C>T
NM_001114086.2:c.541-132C>T	NP_001107558.1:n.541-132C>T
NM_001370649.1:c.-54-132C>T	NP_001357578.1:n.-54-132C>T
NM_001370650.1:c.541-132C>T	NP_001357579.1:n.541-132C>T
NM_016929.5:c.64-132C>T MANE Select	NP_058625.2:n.64-132C>T
NM_001256023.2:c.64-132C>T	NP_001242952.1:n.64-132C>T