Canonical Allele Identifier: CA382021978

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027512A>T (hg19) ; chr11:g.88294344A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294344A>T , CM000673.2:g.88294344A>T	GRCh38
NC_000011.9:g.88027512A>T , CM000673.1:g.88027512A>T	GRCh37
NC_000011.8:g.87667160A>T	NCBI36
NG_007952.1:g.48430T>A , LRG_50:g.48430T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1054T>A MANE Select	ENSP00000227266.4:p.Tyr352Asn
ENST00000533897.2:n.5367T>A
ENST00000676612.1:c.*861T>A	ENSP00000504440.1:n.*861T>A
ENST00000677208.1:c.*560T>A	ENSP00000504347.1:n.*560T>A
ENST00000677661.1:c.*731T>A	ENSP00000503323.1:n.*731T>A
ENST00000677802.1:c.*731T>A	ENSP00000504115.1:n.*731T>A
ENST00000678395.1:c.*560T>A	ENSP00000503123.1:n.*560T>A
ENST00000678464.1:c.1021T>A	ENSP00000503046.1:p.Tyr341Asn
ENST00000678506.1:c.1015T>A	ENSP00000503580.1:p.Tyr339Asn
ENST00000678520.1:c.*705T>A	ENSP00000503361.1:n.*705T>A
ENST00000678554.1:c.889+1789T>A	ENSP00000504541.1:n.889+1789T>A
ENST00000678915.1:c.922T>A	ENSP00000504805.1:p.Tyr308Asn
ENST00000679224.1:c.691T>A	ENSP00000504475.1:p.Tyr231Asn
ENST00000227266.9:c.1054T>A	ENSP00000227266.4:p.Tyr352Asn
ENST00000533897.1:n.3788T>A
NM_001814.4:c.1054T>A , LRG_50t1:c.1054T>A	NP_001805.3:p.Tyr352Asn
NM_001814.5:c.1054T>A	NP_001805.3:p.Tyr352Asn
NM_001814.6:c.1054T>A MANE Select	NP_001805.4:p.Tyr352Asn