Canonical Allele Identifier: CA800941967

Gene: CCT5

Linked Data

• dbSNP Id: rs1467448809
• gnomAD v4: 5-10256166-AGAT-A
• MyVariant Identifiers: chr5:g.10256279_10256281del (hg19) ; chr5:g.10256167_10256169del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256170_10256172del , CM000667.2:g.10256170_10256172del	GRCh38
NC_000005.9:g.10256282_10256284del , CM000667.1:g.10256282_10256284del	GRCh37
NC_000005.8:g.10309282_10309284del	NCBI36
NG_012160.1:g.11001_11003del , LRG_361:g.11001_11003del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.530+17_530+19del MANE Select	ENSP00000280326.4:n.530+17_530+19del
ENST00000280326.8:c.530+17_530+19del	ENSP00000280326.4:n.530+17_530+19del
ENST00000423695.6:n.128-1941_128-1939del
ENST00000503026.5:c.467+17_467+19del	ENSP00000423318.1:n.467+17_467+19del
ENST00000503454.5:c.419+17_419+19del
ENST00000506600.1:c.251+17_251+19del	ENSP00000423052.1:n.251+17_251+19del
ENST00000511700.1:c.445+17_445+19del	ENSP00000423087.1:n.445+17_445+19del
ENST00000512975.5:c.106-1941_106-1939del	ENSP00000425751.1:n.106-1941_106-1939del
ENST00000515390.5:c.365+17_365+19del	ENSP00000426923.1:n.365+17_365+19del
ENST00000515676.5:c.416+17_416+19del	ENSP00000427297.1:n.416+17_416+19del
ENST00000625723.1:c.106-1941_106-1939del	ENSP00000487128.1:n.106-1941_106-1939del
NM_001306153.1:c.467+17_467+19del	NP_001293082.1:n.467+17_467+19del
NM_001306154.1:c.365+17_365+19del	NP_001293083.1:n.365+17_365+19del
NM_001306155.1:c.251+17_251+19del	NP_001293084.1:n.251+17_251+19del
NM_001306156.1:c.416+17_416+19del	NP_001293085.1:n.416+17_416+19del
NM_012073.3:c.530+17_530+19del , LRG_361t1:c.530+17_530+19del	NP_036205.1:n.530+17_530+19del
NM_012073.4:c.530+17_530+19del	NP_036205.1:n.530+17_530+19del
NM_012073.5:c.530+17_530+19del MANE Select	NP_036205.1:n.530+17_530+19del
NM_001306154.2:c.365+17_365+19del	NP_001293083.1:n.365+17_365+19del
NM_001306155.2:c.251+17_251+19del	NP_001293084.1:n.251+17_251+19del
NM_001306156.2:c.416+17_416+19del	NP_001293085.1:n.416+17_416+19del