Canonical Allele Identifier: CA382022049

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027544T>C (hg19) ; chr11:g.88294376T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294376T>C , CM000673.2:g.88294376T>C	GRCh38
NC_000011.9:g.88027544T>C , CM000673.1:g.88027544T>C	GRCh37
NC_000011.8:g.87667192T>C	NCBI36
NG_007952.1:g.48398A>G , LRG_50:g.48398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1022A>G MANE Select	ENSP00000227266.4:p.Tyr341Cys
ENST00000533897.2:n.5335A>G
ENST00000676612.1:c.*829A>G	ENSP00000504440.1:n.*829A>G
ENST00000677208.1:c.*528A>G	ENSP00000504347.1:n.*528A>G
ENST00000677661.1:c.*699A>G	ENSP00000503323.1:n.*699A>G
ENST00000677802.1:c.*699A>G	ENSP00000504115.1:n.*699A>G
ENST00000678395.1:c.*528A>G	ENSP00000503123.1:n.*528A>G
ENST00000678464.1:c.989A>G	ENSP00000503046.1:p.Tyr330Cys
ENST00000678506.1:c.983A>G	ENSP00000503580.1:p.Tyr328Cys
ENST00000678520.1:c.*673A>G	ENSP00000503361.1:n.*673A>G
ENST00000678554.1:c.889+1757A>G	ENSP00000504541.1:n.889+1757A>G
ENST00000678915.1:c.890A>G	ENSP00000504805.1:p.Tyr297Cys
ENST00000679224.1:c.659A>G	ENSP00000504475.1:p.Tyr220Cys
ENST00000227266.9:c.1022A>G	ENSP00000227266.4:p.Tyr341Cys
ENST00000533897.1:n.3756A>G
NM_001814.4:c.1022A>G , LRG_50t1:c.1022A>G	NP_001805.3:p.Tyr341Cys
NM_001814.5:c.1022A>G	NP_001805.3:p.Tyr341Cys
NM_001814.6:c.1022A>G MANE Select	NP_001805.4:p.Tyr341Cys