Canonical Allele Identifier: CA359181559

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256238C>T (hg19) ; chr5:g.10256126C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256126C>T , CM000667.2:g.10256126C>T	GRCh38
NC_000005.9:g.10256238C>T , CM000667.1:g.10256238C>T	GRCh37
NC_000005.8:g.10309238C>T	NCBI36
NG_012160.1:g.10957C>T , LRG_361:g.10957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.503C>T MANE Select	ENSP00000280326.4:p.Thr168Ile
ENST00000280326.8:c.503C>T	ENSP00000280326.4:p.Thr168Ile
ENST00000423695.6:n.128-1985C>T
ENST00000503026.5:c.440C>T	ENSP00000423318.1:p.Thr147Ile
ENST00000503454.5:c.392C>T
ENST00000506600.1:c.224C>T	ENSP00000423052.1:p.Thr75Ile
ENST00000511700.1:c.418C>T	ENSP00000423087.1:n.418C>T
ENST00000512975.5:c.106-1985C>T	ENSP00000425751.1:n.106-1985C>T
ENST00000515390.5:c.338C>T	ENSP00000426923.1:p.Thr113Ile
ENST00000515676.5:c.389C>T	ENSP00000427297.1:p.Thr130Ile
ENST00000625723.1:c.106-1985C>T	ENSP00000487128.1:n.106-1985C>T
NM_001306153.1:c.440C>T	NP_001293082.1:p.Thr147Ile
NM_001306154.1:c.338C>T	NP_001293083.1:p.Thr113Ile
NM_001306155.1:c.224C>T	NP_001293084.1:p.Thr75Ile
NM_001306156.1:c.389C>T	NP_001293085.1:p.Thr130Ile
NM_012073.3:c.503C>T , LRG_361t1:c.503C>T	NP_036205.1:p.Thr168Ile
NM_012073.4:c.503C>T	NP_036205.1:p.Thr168Ile
NM_012073.5:c.503C>T MANE Select	NP_036205.1:p.Thr168Ile
NM_001306154.2:c.338C>T	NP_001293083.1:p.Thr113Ile
NM_001306155.2:c.224C>T	NP_001293084.1:p.Thr75Ile
NM_001306156.2:c.389C>T	NP_001293085.1:p.Thr130Ile