Canonical Allele Identifier: CA1989482753

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294352C= , CM000673.2:g.88294352C=	GRCh38
NC_000011.9:g.88027520C= , CM000673.1:g.88027520C=	GRCh37
NC_000011.8:g.87667168C=	NCBI36
NG_007952.1:g.48422G= , LRG_50:g.48422G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1046G= MANE Select	ENSP00000227266.4:p.Gly349=
ENST00000533897.2:n.5359G=
ENST00000676612.1:c.*853G=	ENSP00000504440.1:n.*853G=
ENST00000677208.1:c.*552G=	ENSP00000504347.1:n.*552G=
ENST00000677661.1:c.*723G=	ENSP00000503323.1:n.*723G=
ENST00000677802.1:c.*723G=	ENSP00000504115.1:n.*723G=
ENST00000678395.1:c.*552G=	ENSP00000503123.1:n.*552G=
ENST00000678464.1:c.1013G=	ENSP00000503046.1:p.Gly338=
ENST00000678506.1:c.1007G=	ENSP00000503580.1:p.Gly336=
ENST00000678520.1:c.*697G=	ENSP00000503361.1:n.*697G=
ENST00000678554.1:c.889+1781G=	ENSP00000504541.1:n.889+1781G=
ENST00000678915.1:c.914G=	ENSP00000504805.1:p.Gly305=
ENST00000679224.1:c.683G=	ENSP00000504475.1:p.Gly228=
ENST00000227266.9:c.1046G=	ENSP00000227266.4:p.Gly349=
ENST00000533897.1:n.3780G=
NM_001814.4:c.1046G= , LRG_50t1:c.1046G=	NP_001805.3:p.Gly349=
NM_001814.5:c.1046G=	NP_001805.3:p.Gly349=
NM_001814.6:c.1046G= MANE Select	NP_001805.4:p.Gly349=