Canonical Allele Identifier: CA359181151

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256111C>T (hg19) ; chr5:g.10255999C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255999C>T , CM000667.2:g.10255999C>T	GRCh38
NC_000005.9:g.10256111C>T , CM000667.1:g.10256111C>T	GRCh37
NC_000005.8:g.10309111C>T	NCBI36
NG_012160.1:g.10830C>T , LRG_361:g.10830C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.376C>T MANE Select	ENSP00000280326.4:p.Arg126Ter
ENST00000280326.8:c.376C>T	ENSP00000280326.4:p.Arg126Ter
ENST00000423695.6:n.128-2112C>T
ENST00000503026.5:c.313C>T	ENSP00000423318.1:p.Arg105Ter
ENST00000503454.5:c.265C>T
ENST00000506600.1:c.97C>T	ENSP00000423052.1:p.Arg33Ter
ENST00000511700.1:c.291C>T	ENSP00000423087.1:n.291C>T
ENST00000512975.5:c.106-2112C>T	ENSP00000425751.1:n.106-2112C>T
ENST00000515390.5:c.211C>T	ENSP00000426923.1:p.Arg71Ter
ENST00000515676.5:c.262C>T	ENSP00000427297.1:p.Arg88Ter
ENST00000625723.1:c.106-2112C>T	ENSP00000487128.1:n.106-2112C>T
NM_001306153.1:c.313C>T	NP_001293082.1:p.Arg105Ter
NM_001306154.1:c.211C>T	NP_001293083.1:p.Arg71Ter
NM_001306155.1:c.97C>T	NP_001293084.1:p.Arg33Ter
NM_001306156.1:c.262C>T	NP_001293085.1:p.Arg88Ter
NM_012073.3:c.376C>T , LRG_361t1:c.376C>T	NP_036205.1:p.Arg126Ter
NM_012073.4:c.376C>T	NP_036205.1:p.Arg126Ter
NM_012073.5:c.376C>T MANE Select	NP_036205.1:p.Arg126Ter
NM_001306154.2:c.211C>T	NP_001293083.1:p.Arg71Ter
NM_001306155.2:c.97C>T	NP_001293084.1:p.Arg33Ter
NM_001306156.2:c.262C>T	NP_001293085.1:p.Arg88Ter