Canonical Allele Identifier: CA1989482779

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294402T= , CM000673.2:g.88294402T=	GRCh38
NC_000011.9:g.88027570T= , CM000673.1:g.88027570T=	GRCh37
NC_000011.8:g.87667218T=	NCBI36
NG_007952.1:g.48372A= , LRG_50:g.48372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.996A= MANE Select	ENSP00000227266.4:p.Lys332=
ENST00000533897.2:n.5309A=
ENST00000676612.1:c.*803A=	ENSP00000504440.1:n.*803A=
ENST00000677208.1:c.*502A=	ENSP00000504347.1:n.*502A=
ENST00000677661.1:c.*673A=	ENSP00000503323.1:n.*673A=
ENST00000677802.1:c.*673A=	ENSP00000504115.1:n.*673A=
ENST00000678395.1:c.*502A=	ENSP00000503123.1:n.*502A=
ENST00000678464.1:c.963A=	ENSP00000503046.1:p.Lys321=
ENST00000678506.1:c.957A=	ENSP00000503580.1:p.Lys319=
ENST00000678520.1:c.*647A=	ENSP00000503361.1:n.*647A=
ENST00000678554.1:c.889+1731A=	ENSP00000504541.1:n.889+1731A=
ENST00000678915.1:c.864A=	ENSP00000504805.1:p.Lys288=
ENST00000679224.1:c.633A=	ENSP00000504475.1:p.Lys211=
ENST00000227266.9:c.996A=	ENSP00000227266.4:p.Lys332=
ENST00000533897.1:n.3730A=
NM_001814.4:c.996A= , LRG_50t1:c.996A=	NP_001805.3:p.Lys332=
NM_001814.5:c.996A=	NP_001805.3:p.Lys332=
NM_001814.6:c.996A= MANE Select	NP_001805.4:p.Lys332=