Canonical Allele Identifier: CA443258207

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256137C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256025C>G , CM000667.2:g.10256025C>G	GRCh38
NC_000005.9:g.10256137C>G , CM000667.1:g.10256137C>G	GRCh37
NC_000005.8:g.10309137C>G	NCBI36
NG_012160.1:g.10856C>G , LRG_361:g.10856C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.402C>G MANE Select	ENSP00000280326.4:p.Ala134=
ENST00000280326.8:c.402C>G	ENSP00000280326.4:p.Ala134=
ENST00000423695.6:n.128-2086C>G
ENST00000503026.5:c.339C>G	ENSP00000423318.1:p.Ala113=
ENST00000503454.5:c.291C>G
ENST00000506600.1:c.123C>G	ENSP00000423052.1:p.Ala41=
ENST00000511700.1:c.317C>G	ENSP00000423087.1:n.317C>G
ENST00000512975.5:c.106-2086C>G	ENSP00000425751.1:n.106-2086C>G
ENST00000515390.5:c.237C>G	ENSP00000426923.1:p.Ala79=
ENST00000515676.5:c.288C>G	ENSP00000427297.1:p.Ala96=
ENST00000625723.1:c.106-2086C>G	ENSP00000487128.1:n.106-2086C>G
NM_001306153.1:c.339C>G	NP_001293082.1:p.Ala113=
NM_001306154.1:c.237C>G	NP_001293083.1:p.Ala79=
NM_001306155.1:c.123C>G	NP_001293084.1:p.Ala41=
NM_001306156.1:c.288C>G	NP_001293085.1:p.Ala96=
NM_012073.3:c.402C>G , LRG_361t1:c.402C>G	NP_036205.1:p.Ala134=
NM_012073.4:c.402C>G	NP_036205.1:p.Ala134=
NM_012073.5:c.402C>G MANE Select	NP_036205.1:p.Ala134=
NM_001306154.2:c.237C>G	NP_001293083.1:p.Ala79=
NM_001306155.2:c.123C>G	NP_001293084.1:p.Ala41=
NM_001306156.2:c.288C>G	NP_001293085.1:p.Ala96=