Canonical Allele Identifier: CA1989482811

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294490G= , CM000673.2:g.88294490G=	GRCh38
NC_000011.9:g.88027658G= , CM000673.1:g.88027658G=	GRCh37
NC_000011.8:g.87667306G=	NCBI36
NG_007952.1:g.48284C= , LRG_50:g.48284C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.908C= MANE Select	ENSP00000227266.4:p.Pro303=
ENST00000533897.2:n.5221C=
ENST00000676612.1:c.*715C=	ENSP00000504440.1:n.*715C=
ENST00000677208.1:c.*414C=	ENSP00000504347.1:n.*414C=
ENST00000677661.1:c.*585C=	ENSP00000503323.1:n.*585C=
ENST00000677802.1:c.*585C=	ENSP00000504115.1:n.*585C=
ENST00000678395.1:c.*414C=	ENSP00000503123.1:n.*414C=
ENST00000678464.1:c.890-15C=	ENSP00000503046.1:n.890-15C=
ENST00000678506.1:c.869C=	ENSP00000503580.1:p.Pro290=
ENST00000678520.1:c.*559C=	ENSP00000503361.1:n.*559C=
ENST00000678554.1:c.889+1643C=	ENSP00000504541.1:n.889+1643C=
ENST00000678915.1:c.776C=	ENSP00000504805.1:p.Pro259=
ENST00000679224.1:c.545C=	ENSP00000504475.1:p.Pro182=
ENST00000227266.9:c.908C=	ENSP00000227266.4:p.Pro303=
ENST00000533897.1:n.3642C=
NM_001814.4:c.908C= , LRG_50t1:c.908C=	NP_001805.3:p.Pro303=
NM_001814.5:c.908C=	NP_001805.3:p.Pro303=
NM_001814.6:c.908C= MANE Select	NP_001805.4:p.Pro303=