Canonical Allele Identifier: CA1989482746

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294340C= , CM000673.2:g.88294340C=	GRCh38
NC_000011.9:g.88027508C= , CM000673.1:g.88027508C=	GRCh37
NC_000011.8:g.87667156C=	NCBI36
NG_007952.1:g.48434G= , LRG_50:g.48434G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1058G= MANE Select	ENSP00000227266.4:p.Gly353=
ENST00000533897.2:n.5371G=
ENST00000676612.1:c.*865G=	ENSP00000504440.1:n.*865G=
ENST00000677208.1:c.*564G=	ENSP00000504347.1:n.*564G=
ENST00000677661.1:c.*735G=	ENSP00000503323.1:n.*735G=
ENST00000677802.1:c.*735G=	ENSP00000504115.1:n.*735G=
ENST00000678395.1:c.*564G=	ENSP00000503123.1:n.*564G=
ENST00000678464.1:c.1025G=	ENSP00000503046.1:p.Gly342=
ENST00000678506.1:c.1019G=	ENSP00000503580.1:p.Gly340=
ENST00000678520.1:c.*709G=	ENSP00000503361.1:n.*709G=
ENST00000678554.1:c.889+1793G=	ENSP00000504541.1:n.889+1793G=
ENST00000678915.1:c.926G=	ENSP00000504805.1:p.Gly309=
ENST00000679224.1:c.695G=	ENSP00000504475.1:p.Gly232=
ENST00000227266.9:c.1058G=	ENSP00000227266.4:p.Gly353=
ENST00000533897.1:n.3792G=
NM_001814.4:c.1058G= , LRG_50t1:c.1058G=	NP_001805.3:p.Gly353=
NM_001814.5:c.1058G=	NP_001805.3:p.Gly353=
NM_001814.6:c.1058G= MANE Select	NP_001805.4:p.Gly353=