Canonical Allele Identifier: CA359181265

Gene: CCT5

Linked Data

• MyVariant Identifiers: chr5:g.10256145A>C (hg19) ; chr5:g.10256033A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10256033A>C , CM000667.2:g.10256033A>C	GRCh38
NC_000005.9:g.10256145A>C , CM000667.1:g.10256145A>C	GRCh37
NC_000005.8:g.10309145A>C	NCBI36
NG_012160.1:g.10864A>C , LRG_361:g.10864A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280326.9:c.410A>C MANE Select	ENSP00000280326.4:p.Tyr137Ser
ENST00000280326.8:c.410A>C	ENSP00000280326.4:p.Tyr137Ser
ENST00000423695.6:n.128-2078A>C
ENST00000503026.5:c.347A>C	ENSP00000423318.1:p.Tyr116Ser
ENST00000503454.5:c.299A>C
ENST00000506600.1:c.131A>C	ENSP00000423052.1:p.Tyr44Ser
ENST00000511700.1:c.325A>C	ENSP00000423087.1:n.325A>C
ENST00000512975.5:c.106-2078A>C	ENSP00000425751.1:n.106-2078A>C
ENST00000515390.5:c.245A>C	ENSP00000426923.1:p.Tyr82Ser
ENST00000515676.5:c.296A>C	ENSP00000427297.1:p.Tyr99Ser
ENST00000625723.1:c.106-2078A>C	ENSP00000487128.1:n.106-2078A>C
NM_001306153.1:c.347A>C	NP_001293082.1:p.Tyr116Ser
NM_001306154.1:c.245A>C	NP_001293083.1:p.Tyr82Ser
NM_001306155.1:c.131A>C	NP_001293084.1:p.Tyr44Ser
NM_001306156.1:c.296A>C	NP_001293085.1:p.Tyr99Ser
NM_012073.3:c.410A>C , LRG_361t1:c.410A>C	NP_036205.1:p.Tyr137Ser
NM_012073.4:c.410A>C	NP_036205.1:p.Tyr137Ser
NM_012073.5:c.410A>C MANE Select	NP_036205.1:p.Tyr137Ser
NM_001306154.2:c.245A>C	NP_001293083.1:p.Tyr82Ser
NM_001306155.2:c.131A>C	NP_001293084.1:p.Tyr44Ser
NM_001306156.2:c.296A>C	NP_001293085.1:p.Tyr99Ser