Canonical Allele Identifier: CA443258259

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256155T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256043T>A , CM000667.2:g.10256043T>A	GRCh38
NC_000005.9:g.10256155T>A , CM000667.1:g.10256155T>A	GRCh37
NC_000005.8:g.10309155T>A	NCBI36
NG_012160.1:g.10874T>A , LRG_361:g.10874T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.420T>A MANE Select	ENSP00000280326.4:p.Ala140=
ENST00000280326.8:c.420T>A	ENSP00000280326.4:p.Ala140=
ENST00000423695.6:n.128-2068T>A
ENST00000503026.5:c.357T>A	ENSP00000423318.1:p.Ala119=
ENST00000503454.5:c.309T>A
ENST00000506600.1:c.141T>A	ENSP00000423052.1:p.Ala47=
ENST00000511700.1:c.335T>A	ENSP00000423087.1:n.335T>A
ENST00000512975.5:c.106-2068T>A	ENSP00000425751.1:n.106-2068T>A
ENST00000515390.5:c.255T>A	ENSP00000426923.1:p.Ala85=
ENST00000515676.5:c.306T>A	ENSP00000427297.1:p.Ala102=
ENST00000625723.1:c.106-2068T>A	ENSP00000487128.1:n.106-2068T>A
NM_001306153.1:c.357T>A	NP_001293082.1:p.Ala119=
NM_001306154.1:c.255T>A	NP_001293083.1:p.Ala85=
NM_001306155.1:c.141T>A	NP_001293084.1:p.Ala47=
NM_001306156.1:c.306T>A	NP_001293085.1:p.Ala102=
NM_012073.3:c.420T>A , LRG_361t1:c.420T>A	NP_036205.1:p.Ala140=
NM_012073.4:c.420T>A	NP_036205.1:p.Ala140=
NM_012073.5:c.420T>A MANE Select	NP_036205.1:p.Ala140=
NM_001306154.2:c.255T>A	NP_001293083.1:p.Ala85=
NM_001306155.2:c.141T>A	NP_001293084.1:p.Ala47=
NM_001306156.2:c.306T>A	NP_001293085.1:p.Ala102=