Canonical Allele Identifier: CA1989482743

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294334C= , CM000673.2:g.88294334C=	GRCh38
NC_000011.9:g.88027502C= , CM000673.1:g.88027502C=	GRCh37
NC_000011.8:g.87667150C=	NCBI36
NG_007952.1:g.48440G= , LRG_50:g.48440G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1064G= MANE Select	ENSP00000227266.4:p.Cys355=
ENST00000533897.2:n.5377G=
ENST00000676612.1:c.*871G=	ENSP00000504440.1:n.*871G=
ENST00000677208.1:c.*570G=	ENSP00000504347.1:n.*570G=
ENST00000677661.1:c.*741G=	ENSP00000503323.1:n.*741G=
ENST00000677802.1:c.*741G=	ENSP00000504115.1:n.*741G=
ENST00000678395.1:c.*570G=	ENSP00000503123.1:n.*570G=
ENST00000678464.1:c.1031G=	ENSP00000503046.1:p.Cys344=
ENST00000678506.1:c.1025G=	ENSP00000503580.1:p.Cys342=
ENST00000678520.1:c.*715G=	ENSP00000503361.1:n.*715G=
ENST00000678554.1:c.889+1799G=	ENSP00000504541.1:n.889+1799G=
ENST00000678915.1:c.932G=	ENSP00000504805.1:p.Cys311=
ENST00000679224.1:c.701G=	ENSP00000504475.1:p.Cys234=
ENST00000227266.9:c.1064G=	ENSP00000227266.4:p.Cys355=
ENST00000533897.1:n.3798G=
NM_001814.4:c.1064G= , LRG_50t1:c.1064G=	NP_001805.3:p.Cys355=
NM_001814.5:c.1064G=	NP_001805.3:p.Cys355=
NM_001814.6:c.1064G= MANE Select	NP_001805.4:p.Cys355=