Canonical Allele Identifier: CA1989482809

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294486G= , CM000673.2:g.88294486G=	GRCh38
NC_000011.9:g.88027654G= , CM000673.1:g.88027654G=	GRCh37
NC_000011.8:g.87667302G=	NCBI36
NG_007952.1:g.48288C= , LRG_50:g.48288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.912C= MANE Select	ENSP00000227266.4:p.Tyr304=
ENST00000533897.2:n.5225C=
ENST00000676612.1:c.*719C=	ENSP00000504440.1:n.*719C=
ENST00000677208.1:c.*418C=	ENSP00000504347.1:n.*418C=
ENST00000677661.1:c.*589C=	ENSP00000503323.1:n.*589C=
ENST00000677802.1:c.*589C=	ENSP00000504115.1:n.*589C=
ENST00000678395.1:c.*418C=	ENSP00000503123.1:n.*418C=
ENST00000678464.1:c.890-11C=	ENSP00000503046.1:n.890-11C=
ENST00000678506.1:c.873C=	ENSP00000503580.1:p.Tyr291=
ENST00000678520.1:c.*563C=	ENSP00000503361.1:n.*563C=
ENST00000678554.1:c.889+1647C=	ENSP00000504541.1:n.889+1647C=
ENST00000678915.1:c.780C=	ENSP00000504805.1:p.Tyr260=
ENST00000679224.1:c.549C=	ENSP00000504475.1:p.Tyr183=
ENST00000227266.9:c.912C=	ENSP00000227266.4:p.Tyr304=
ENST00000533897.1:n.3646C=
NM_001814.4:c.912C= , LRG_50t1:c.912C=	NP_001805.3:p.Tyr304=
NM_001814.5:c.912C=	NP_001805.3:p.Tyr304=
NM_001814.6:c.912C= MANE Select	NP_001805.4:p.Tyr304=