Canonical Allele Identifier: CA359181146

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256110C>A (hg19) ; chr5:g.10255998C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255998C>A , CM000667.2:g.10255998C>A	GRCh38
NC_000005.9:g.10256110C>A , CM000667.1:g.10256110C>A	GRCh37
NC_000005.8:g.10309110C>A	NCBI36
NG_012160.1:g.10829C>A , LRG_361:g.10829C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.375C>A MANE Select	ENSP00000280326.4:p.Asp125Glu
ENST00000280326.8:c.375C>A	ENSP00000280326.4:p.Asp125Glu
ENST00000423695.6:n.128-2113C>A
ENST00000503026.5:c.312C>A	ENSP00000423318.1:p.Asp104Glu
ENST00000503454.5:c.264C>A
ENST00000506600.1:c.96C>A	ENSP00000423052.1:p.Asp32Glu
ENST00000511700.1:c.290C>A	ENSP00000423087.1:n.290C>A
ENST00000512975.5:c.106-2113C>A	ENSP00000425751.1:n.106-2113C>A
ENST00000515390.5:c.210C>A	ENSP00000426923.1:p.Asp70Glu
ENST00000515676.5:c.261C>A	ENSP00000427297.1:p.Asp87Glu
ENST00000625723.1:c.106-2113C>A	ENSP00000487128.1:n.106-2113C>A
NM_001306153.1:c.312C>A	NP_001293082.1:p.Asp104Glu
NM_001306154.1:c.210C>A	NP_001293083.1:p.Asp70Glu
NM_001306155.1:c.96C>A	NP_001293084.1:p.Asp32Glu
NM_001306156.1:c.261C>A	NP_001293085.1:p.Asp87Glu
NM_012073.3:c.375C>A , LRG_361t1:c.375C>A	NP_036205.1:p.Asp125Glu
NM_012073.4:c.375C>A	NP_036205.1:p.Asp125Glu
NM_012073.5:c.375C>A MANE Select	NP_036205.1:p.Asp125Glu
NM_001306154.2:c.210C>A	NP_001293083.1:p.Asp70Glu
NM_001306155.2:c.96C>A	NP_001293084.1:p.Asp32Glu
NM_001306156.2:c.261C>A	NP_001293085.1:p.Asp87Glu