Canonical Allele Identifier: CA1989489451

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88309176G= , CM000673.2:g.88309176G=	GRCh38
NC_000011.9:g.88042344G= , CM000673.1:g.88042344G=	GRCh37
NC_000011.8:g.87681992G=	NCBI36
NG_007952.1:g.33598C= , LRG_50:g.33598C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.628C= MANE Select	NP_001805.4:p.Arg210=
ENST00000227266.10:c.628C= MANE Select	ENSP00000227266.4:p.Arg210=
NM_001814.4:c.628C= , LRG_50t1:c.628C=	NP_001805.3:p.Arg210=
NM_001814.5:c.628C=	NP_001805.3:p.Arg210=
ENST00000227266.9:c.628C=	ENSP00000227266.4:p.Arg210=
ENST00000527018.5:c.498C=
ENST00000527018.6:c.628C=	ENSP00000432556.2:p.Arg210=
ENST00000533897.2:n.676C=
ENST00000676612.1:c.*435C=	ENSP00000504440.1:n.*435C=
ENST00000677208.1:c.*134C=	ENSP00000504347.1:n.*134C=
ENST00000677661.1:c.*305C=	ENSP00000503323.1:n.*305C=
ENST00000677802.1:c.*305C=	ENSP00000504115.1:n.*305C=
ENST00000678065.1:n.188C=
ENST00000678395.1:c.*134C=	ENSP00000503123.1:n.*134C=
ENST00000678464.1:c.628C=	ENSP00000503046.1:p.Arg210=
ENST00000678506.1:c.589C=	ENSP00000503580.1:p.Arg197=
ENST00000678520.1:c.*292+3212C=	ENSP00000503361.1:n.*292+3212C=
ENST00000678554.1:c.628C=	ENSP00000504541.1:p.Arg210=
ENST00000678915.1:c.628C=	ENSP00000504805.1:p.Arg210=
ENST00000679224.1:c.265C=	ENSP00000504475.1:p.Arg89=