Canonical Allele Identifier: CA359181588

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256249A>T (hg19) ; chr5:g.10256137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256137A>T , CM000667.2:g.10256137A>T	GRCh38
NC_000005.9:g.10256249A>T , CM000667.1:g.10256249A>T	GRCh37
NC_000005.8:g.10309249A>T	NCBI36
NG_012160.1:g.10968A>T , LRG_361:g.10968A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.514A>T MANE Select	ENSP00000280326.4:p.Thr172Ser
ENST00000280326.8:c.514A>T	ENSP00000280326.4:p.Thr172Ser
ENST00000423695.6:n.128-1974A>T
ENST00000503026.5:c.451A>T	ENSP00000423318.1:p.Thr151Ser
ENST00000503454.5:c.403A>T
ENST00000506600.1:c.235A>T	ENSP00000423052.1:p.Thr79Ser
ENST00000511700.1:c.429A>T	ENSP00000423087.1:n.429A>T
ENST00000512975.5:c.106-1974A>T	ENSP00000425751.1:n.106-1974A>T
ENST00000515390.5:c.349A>T	ENSP00000426923.1:p.Thr117Ser
ENST00000515676.5:c.400A>T	ENSP00000427297.1:p.Thr134Ser
ENST00000625723.1:c.106-1974A>T	ENSP00000487128.1:n.106-1974A>T
NM_001306153.1:c.451A>T	NP_001293082.1:p.Thr151Ser
NM_001306154.1:c.349A>T	NP_001293083.1:p.Thr117Ser
NM_001306155.1:c.235A>T	NP_001293084.1:p.Thr79Ser
NM_001306156.1:c.400A>T	NP_001293085.1:p.Thr134Ser
NM_012073.3:c.514A>T , LRG_361t1:c.514A>T	NP_036205.1:p.Thr172Ser
NM_012073.4:c.514A>T	NP_036205.1:p.Thr172Ser
NM_012073.5:c.514A>T MANE Select	NP_036205.1:p.Thr172Ser
NM_001306154.2:c.349A>T	NP_001293083.1:p.Thr117Ser
NM_001306155.2:c.235A>T	NP_001293084.1:p.Thr79Ser
NM_001306156.2:c.400A>T	NP_001293085.1:p.Thr134Ser