Canonical Allele Identifier: CA382021902

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027478T>A (hg19) ; chr11:g.88294310T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294310T>A , CM000673.2:g.88294310T>A	GRCh38
NC_000011.9:g.88027478T>A , CM000673.1:g.88027478T>A	GRCh37
NC_000011.8:g.87667126T>A	NCBI36
NG_007952.1:g.48464A>T , LRG_50:g.48464A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1088A>T MANE Select	ENSP00000227266.4:p.Glu363Val
ENST00000533897.2:n.5401A>T
ENST00000676612.1:c.*895A>T	ENSP00000504440.1:n.*895A>T
ENST00000677208.1:c.*594A>T	ENSP00000504347.1:n.*594A>T
ENST00000677661.1:c.*765A>T	ENSP00000503323.1:n.*765A>T
ENST00000677802.1:c.*765A>T	ENSP00000504115.1:n.*765A>T
ENST00000678395.1:c.*594A>T	ENSP00000503123.1:n.*594A>T
ENST00000678464.1:c.1055A>T	ENSP00000503046.1:p.Glu352Val
ENST00000678506.1:c.1049A>T	ENSP00000503580.1:p.Glu350Val
ENST00000678520.1:c.*739A>T	ENSP00000503361.1:n.*739A>T
ENST00000678554.1:c.889+1823A>T	ENSP00000504541.1:n.889+1823A>T
ENST00000678915.1:c.956A>T	ENSP00000504805.1:p.Glu319Val
ENST00000679224.1:c.725A>T	ENSP00000504475.1:p.Glu242Val
ENST00000227266.9:c.1088A>T	ENSP00000227266.4:p.Glu363Val
ENST00000533897.1:n.3822A>T
NM_001814.4:c.1088A>T , LRG_50t1:c.1088A>T	NP_001805.3:p.Glu363Val
NM_001814.5:c.1088A>T	NP_001805.3:p.Glu363Val
NM_001814.6:c.1088A>T MANE Select	NP_001805.4:p.Glu363Val