Canonical Allele Identifier: CA443258001

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256081T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10255969T>C , CM000667.2:g.10255969T>C	GRCh38
NC_000005.9:g.10256081T>C , CM000667.1:g.10256081T>C	GRCh37
NC_000005.8:g.10309081T>C	NCBI36
NG_012160.1:g.10800T>C , LRG_361:g.10800T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.346T>C MANE Select	ENSP00000280326.4:p.Leu116=
ENST00000280326.8:c.346T>C	ENSP00000280326.4:p.Leu116=
ENST00000423695.6:n.128-2142T>C
ENST00000503026.5:c.283T>C	ENSP00000423318.1:p.Leu95=
ENST00000503454.5:c.235T>C
ENST00000506600.1:c.67T>C	ENSP00000423052.1:p.Leu23=
ENST00000511700.1:c.261T>C	ENSP00000423087.1:p.Pro87=
ENST00000512975.5:c.106-2142T>C	ENSP00000425751.1:n.106-2142T>C
ENST00000515390.5:c.181T>C	ENSP00000426923.1:p.Leu61=
ENST00000515676.5:c.232T>C	ENSP00000427297.1:p.Leu78=
ENST00000625723.1:c.106-2142T>C	ENSP00000487128.1:n.106-2142T>C
NM_001306153.1:c.283T>C	NP_001293082.1:p.Leu95=
NM_001306154.1:c.181T>C	NP_001293083.1:p.Leu61=
NM_001306155.1:c.67T>C	NP_001293084.1:p.Leu23=
NM_001306156.1:c.232T>C	NP_001293085.1:p.Leu78=
NM_012073.3:c.346T>C , LRG_361t1:c.346T>C	NP_036205.1:p.Leu116=
NM_012073.4:c.346T>C	NP_036205.1:p.Leu116=
NM_012073.5:c.346T>C MANE Select	NP_036205.1:p.Leu116=
NM_001306154.2:c.181T>C	NP_001293083.1:p.Leu61=
NM_001306155.2:c.67T>C	NP_001293084.1:p.Leu23=
NM_001306156.2:c.232T>C	NP_001293085.1:p.Leu78=