Canonical Allele Identifier: CA1989490962

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88312463A= , CM000673.2:g.88312463A=	GRCh38
NC_000011.9:g.88045631A= , CM000673.1:g.88045631A=	GRCh37
NC_000011.8:g.87685279A=	NCBI36
NG_007952.1:g.30311T= , LRG_50:g.30311T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.410T= MANE Select	ENSP00000227266.4:p.Phe137=
ENST00000527018.6:c.410T=	ENSP00000432556.2:p.Phe137=
ENST00000533897.2:n.458T=
ENST00000676612.1:c.*217T=	ENSP00000504440.1:n.*217T=
ENST00000677208.1:c.319-3145T=	ENSP00000504347.1:n.319-3145T=
ENST00000677661.1:c.*87T=	ENSP00000503323.1:n.*87T=
ENST00000677802.1:c.*87T=	ENSP00000504115.1:n.*87T=
ENST00000678395.1:c.410T=	ENSP00000503123.1:p.Phe137=
ENST00000678464.1:c.410T=	ENSP00000503046.1:p.Phe137=
ENST00000678506.1:c.410T=	ENSP00000503580.1:p.Phe137=
ENST00000678520.1:c.*217T=	ENSP00000503361.1:n.*217T=
ENST00000678554.1:c.410T=	ENSP00000504541.1:p.Phe137=
ENST00000678915.1:c.410T=	ENSP00000504805.1:p.Phe137=
ENST00000679224.1:c.47T=	ENSP00000504475.1:p.Phe16=
ENST00000227266.9:c.410T=	ENSP00000227266.4:p.Phe137=
ENST00000527018.5:c.280T=
ENST00000533865.5:n.432T=
NM_001814.4:c.410T= , LRG_50t1:c.410T=	NP_001805.3:p.Phe137=
NM_001814.5:c.410T=	NP_001805.3:p.Phe137=
NM_001814.6:c.410T= MANE Select	NP_001805.4:p.Phe137=