Canonical Allele Identifier: CA557542349
Gene: CCT5 HGNC NCBI

Linked Data

dbSNP Id: rs1561046660

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10256175_10256177dup , CM000667.2:g.10256175_10256177dup GRCh38
NC_000005.9:g.10256287_10256289dup , CM000667.1:g.10256287_10256289dup GRCh37
NC_000005.8:g.10309287_10309289dup NCBI36
NG_012160.1:g.11006_11008dup , LRG_361:g.11006_11008dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000280326.9:c.530+22_530+24dup MANE Select ENSP00000280326.4:n.530+22_530+24dup
ENST00000280326.8:c.530+22_530+24dup ENSP00000280326.4:n.530+22_530+24dup
ENST00000423695.6:n.128-1936_128-1934dup
ENST00000503026.5:c.467+22_467+24dup ENSP00000423318.1:n.467+22_467+24dup
ENST00000503454.5:c.419+22_419+24dup
ENST00000506600.1:c.251+22_251+24dup ENSP00000423052.1:n.251+22_251+24dup
ENST00000511700.1:c.445+22_445+24dup ENSP00000423087.1:n.445+22_445+24dup
ENST00000512975.5:c.106-1936_106-1934dup ENSP00000425751.1:n.106-1936_106-1934dup
ENST00000515390.5:c.365+22_365+24dup ENSP00000426923.1:n.365+22_365+24dup
ENST00000515676.5:c.416+22_416+24dup ENSP00000427297.1:n.416+22_416+24dup
ENST00000625723.1:c.106-1936_106-1934dup ENSP00000487128.1:n.106-1936_106-1934dup
NM_001306153.1:c.467+22_467+24dup NP_001293082.1:n.467+22_467+24dup
NM_001306154.1:c.365+22_365+24dup NP_001293083.1:n.365+22_365+24dup
NM_001306155.1:c.251+22_251+24dup NP_001293084.1:n.251+22_251+24dup
NM_001306156.1:c.416+22_416+24dup NP_001293085.1:n.416+22_416+24dup
NM_012073.3:c.530+22_530+24dup , LRG_361t1:c.530+22_530+24dup NP_036205.1:n.530+22_530+24dup
NM_012073.4:c.530+22_530+24dup NP_036205.1:n.530+22_530+24dup
NM_012073.5:c.530+22_530+24dup MANE Select NP_036205.1:n.530+22_530+24dup
NM_001306154.2:c.365+22_365+24dup NP_001293083.1:n.365+22_365+24dup
NM_001306155.2:c.251+22_251+24dup NP_001293084.1:n.251+22_251+24dup
NM_001306156.2:c.416+22_416+24dup NP_001293085.1:n.416+22_416+24dup