Canonical Allele Identifier: CA382022023

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027533A>T (hg19) ; chr11:g.88294365A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294365A>T , CM000673.2:g.88294365A>T	GRCh38
NC_000011.9:g.88027533A>T , CM000673.1:g.88027533A>T	GRCh37
NC_000011.8:g.87667181A>T	NCBI36
NG_007952.1:g.48409T>A , LRG_50:g.48409T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1033T>A MANE Select	ENSP00000227266.4:p.Tyr345Asn
ENST00000533897.2:n.5346T>A
ENST00000676612.1:c.*840T>A	ENSP00000504440.1:n.*840T>A
ENST00000677208.1:c.*539T>A	ENSP00000504347.1:n.*539T>A
ENST00000677661.1:c.*710T>A	ENSP00000503323.1:n.*710T>A
ENST00000677802.1:c.*710T>A	ENSP00000504115.1:n.*710T>A
ENST00000678395.1:c.*539T>A	ENSP00000503123.1:n.*539T>A
ENST00000678464.1:c.1000T>A	ENSP00000503046.1:p.Tyr334Asn
ENST00000678506.1:c.994T>A	ENSP00000503580.1:p.Tyr332Asn
ENST00000678520.1:c.*684T>A	ENSP00000503361.1:n.*684T>A
ENST00000678554.1:c.889+1768T>A	ENSP00000504541.1:n.889+1768T>A
ENST00000678915.1:c.901T>A	ENSP00000504805.1:p.Tyr301Asn
ENST00000679224.1:c.670T>A	ENSP00000504475.1:p.Tyr224Asn
ENST00000227266.9:c.1033T>A	ENSP00000227266.4:p.Tyr345Asn
ENST00000533897.1:n.3767T>A
NM_001814.4:c.1033T>A , LRG_50t1:c.1033T>A	NP_001805.3:p.Tyr345Asn
NM_001814.5:c.1033T>A	NP_001805.3:p.Tyr345Asn
NM_001814.6:c.1033T>A MANE Select	NP_001805.4:p.Tyr345Asn