Canonical Allele Identifier: CA359181392

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256187T>A (hg19) ; chr5:g.10256075T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256075T>A , CM000667.2:g.10256075T>A	GRCh38
NC_000005.9:g.10256187T>A , CM000667.1:g.10256187T>A	GRCh37
NC_000005.8:g.10309187T>A	NCBI36
NG_012160.1:g.10906T>A , LRG_361:g.10906T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000280326.9:c.452T>A MANE Select	ENSP00000280326.4:p.Ile151Asn
ENST00000280326.8:c.452T>A	ENSP00000280326.4:p.Ile151Asn
ENST00000423695.6:n.128-2036T>A
ENST00000503026.5:c.389T>A	ENSP00000423318.1:p.Ile130Asn
ENST00000503454.5:c.341T>A
ENST00000506600.1:c.173T>A	ENSP00000423052.1:p.Ile58Asn
ENST00000511700.1:c.367T>A	ENSP00000423087.1:n.367T>A
ENST00000512975.5:c.106-2036T>A	ENSP00000425751.1:n.106-2036T>A
ENST00000515390.5:c.287T>A	ENSP00000426923.1:p.Ile96Asn
ENST00000515676.5:c.338T>A	ENSP00000427297.1:p.Ile113Asn
ENST00000625723.1:c.106-2036T>A	ENSP00000487128.1:n.106-2036T>A
NM_001306153.1:c.389T>A	NP_001293082.1:p.Ile130Asn
NM_001306154.1:c.287T>A	NP_001293083.1:p.Ile96Asn
NM_001306155.1:c.173T>A	NP_001293084.1:p.Ile58Asn
NM_001306156.1:c.338T>A	NP_001293085.1:p.Ile113Asn
NM_012073.3:c.452T>A , LRG_361t1:c.452T>A	NP_036205.1:p.Ile151Asn
NM_012073.4:c.452T>A	NP_036205.1:p.Ile151Asn
NM_012073.5:c.452T>A MANE Select	NP_036205.1:p.Ile151Asn
NM_001306154.2:c.287T>A	NP_001293083.1:p.Ile96Asn
NM_001306155.2:c.173T>A	NP_001293084.1:p.Ile58Asn
NM_001306156.2:c.338T>A	NP_001293085.1:p.Ile113Asn