Canonical Allele Identifier: CA359181561

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256240G>C (hg19) ; chr5:g.10256128G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256128G>C , CM000667.2:g.10256128G>C	GRCh38
NC_000005.9:g.10256240G>C , CM000667.1:g.10256240G>C	GRCh37
NC_000005.8:g.10309240G>C	NCBI36
NG_012160.1:g.10959G>C , LRG_361:g.10959G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.505G>C MANE Select	ENSP00000280326.4:p.Ala169Pro
ENST00000280326.8:c.505G>C	ENSP00000280326.4:p.Ala169Pro
ENST00000423695.6:n.128-1983G>C
ENST00000503026.5:c.442G>C	ENSP00000423318.1:p.Ala148Pro
ENST00000503454.5:c.394G>C
ENST00000506600.1:c.226G>C	ENSP00000423052.1:p.Ala76Pro
ENST00000511700.1:c.420G>C	ENSP00000423087.1:n.420G>C
ENST00000512975.5:c.106-1983G>C	ENSP00000425751.1:n.106-1983G>C
ENST00000515390.5:c.340G>C	ENSP00000426923.1:p.Ala114Pro
ENST00000515676.5:c.391G>C	ENSP00000427297.1:p.Ala131Pro
ENST00000625723.1:c.106-1983G>C	ENSP00000487128.1:n.106-1983G>C
NM_001306153.1:c.442G>C	NP_001293082.1:p.Ala148Pro
NM_001306154.1:c.340G>C	NP_001293083.1:p.Ala114Pro
NM_001306155.1:c.226G>C	NP_001293084.1:p.Ala76Pro
NM_001306156.1:c.391G>C	NP_001293085.1:p.Ala131Pro
NM_012073.3:c.505G>C , LRG_361t1:c.505G>C	NP_036205.1:p.Ala169Pro
NM_012073.4:c.505G>C	NP_036205.1:p.Ala169Pro
NM_012073.5:c.505G>C MANE Select	NP_036205.1:p.Ala169Pro
NM_001306154.2:c.340G>C	NP_001293083.1:p.Ala114Pro
NM_001306155.2:c.226G>C	NP_001293084.1:p.Ala76Pro
NM_001306156.2:c.391G>C	NP_001293085.1:p.Ala131Pro