Canonical Allele Identifier: CA1989482824

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294520T= , CM000673.2:g.88294520T=	GRCh38
NC_000011.9:g.88027688T= , CM000673.1:g.88027688T=	GRCh37
NC_000011.8:g.87667336T=	NCBI36
NG_007952.1:g.48254A= , LRG_50:g.48254A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.890-12A= MANE Select	ENSP00000227266.4:n.890-12A=
ENST00000533897.2:n.5203-12A=
ENST00000676612.1:c.*697-12A=	ENSP00000504440.1:n.*697-12A=
ENST00000677208.1:c.*396-12A=	ENSP00000504347.1:n.*396-12A=
ENST00000677661.1:c.*567-12A=	ENSP00000503323.1:n.*567-12A=
ENST00000677802.1:c.*567-12A=	ENSP00000504115.1:n.*567-12A=
ENST00000678395.1:c.*396-12A=	ENSP00000503123.1:n.*396-12A=
ENST00000678464.1:c.890-45A=	ENSP00000503046.1:n.890-45A=
ENST00000678506.1:c.851-12A=	ENSP00000503580.1:n.851-12A=
ENST00000678520.1:c.*541-12A=	ENSP00000503361.1:n.*541-12A=
ENST00000678554.1:c.889+1613A=	ENSP00000504541.1:n.889+1613A=
ENST00000678915.1:c.758-12A=	ENSP00000504805.1:n.758-12A=
ENST00000679224.1:c.527-12A=	ENSP00000504475.1:n.527-12A=
ENST00000227266.9:c.890-12A=	ENSP00000227266.4:n.890-12A=
ENST00000533897.1:n.3624-12A=
NM_001814.4:c.890-12A= , LRG_50t1:c.890-12A=	NP_001805.3:n.890-12A=
NM_001814.5:c.890-12A=	NP_001805.3:n.890-12A=
NM_001814.6:c.890-12A= MANE Select	NP_001805.4:n.890-12A=