Canonical Allele Identifier: CA1989482778

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294401T= , CM000673.2:g.88294401T=	GRCh38
NC_000011.9:g.88027569T= , CM000673.1:g.88027569T=	GRCh37
NC_000011.8:g.87667217T=	NCBI36
NG_007952.1:g.48373A= , LRG_50:g.48373A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.997A= MANE Select	ENSP00000227266.4:p.Met333=
ENST00000533897.2:n.5310A=
ENST00000676612.1:c.*804A=	ENSP00000504440.1:n.*804A=
ENST00000677208.1:c.*503A=	ENSP00000504347.1:n.*503A=
ENST00000677661.1:c.*674A=	ENSP00000503323.1:n.*674A=
ENST00000677802.1:c.*674A=	ENSP00000504115.1:n.*674A=
ENST00000678395.1:c.*503A=	ENSP00000503123.1:n.*503A=
ENST00000678464.1:c.964A=	ENSP00000503046.1:p.Met322=
ENST00000678506.1:c.958A=	ENSP00000503580.1:p.Met320=
ENST00000678520.1:c.*648A=	ENSP00000503361.1:n.*648A=
ENST00000678554.1:c.889+1732A=	ENSP00000504541.1:n.889+1732A=
ENST00000678915.1:c.865A=	ENSP00000504805.1:p.Met289=
ENST00000679224.1:c.634A=	ENSP00000504475.1:p.Met212=
ENST00000227266.9:c.997A=	ENSP00000227266.4:p.Met333=
ENST00000533897.1:n.3731A=
NM_001814.4:c.997A= , LRG_50t1:c.997A=	NP_001805.3:p.Met333=
NM_001814.5:c.997A=	NP_001805.3:p.Met333=
NM_001814.6:c.997A= MANE Select	NP_001805.4:p.Met333=