Canonical Allele Identifier: CA1989482792

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294444T= , CM000673.2:g.88294444T=	GRCh38
NC_000011.9:g.88027612T= , CM000673.1:g.88027612T=	GRCh37
NC_000011.8:g.87667260T=	NCBI36
NG_007952.1:g.48330A= , LRG_50:g.48330A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.954A= MANE Select	ENSP00000227266.4:p.Glu318=
ENST00000533897.2:n.5267A=
ENST00000676612.1:c.*761A=	ENSP00000504440.1:n.*761A=
ENST00000677208.1:c.*460A=	ENSP00000504347.1:n.*460A=
ENST00000677661.1:c.*631A=	ENSP00000503323.1:n.*631A=
ENST00000677802.1:c.*631A=	ENSP00000504115.1:n.*631A=
ENST00000678395.1:c.*460A=	ENSP00000503123.1:n.*460A=
ENST00000678464.1:c.921A=	ENSP00000503046.1:p.Glu307=
ENST00000678506.1:c.915A=	ENSP00000503580.1:p.Glu305=
ENST00000678520.1:c.*605A=	ENSP00000503361.1:n.*605A=
ENST00000678554.1:c.889+1689A=	ENSP00000504541.1:n.889+1689A=
ENST00000678915.1:c.822A=	ENSP00000504805.1:p.Glu274=
ENST00000679224.1:c.591A=	ENSP00000504475.1:p.Glu197=
ENST00000227266.9:c.954A=	ENSP00000227266.4:p.Glu318=
ENST00000533897.1:n.3688A=
NM_001814.4:c.954A= , LRG_50t1:c.954A=	NP_001805.3:p.Glu318=
NM_001814.5:c.954A=	NP_001805.3:p.Glu318=
NM_001814.6:c.954A= MANE Select	NP_001805.4:p.Glu318=