Canonical Allele Identifier: CA1989482798

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294464G= , CM000673.2:g.88294464G=	GRCh38
NC_000011.9:g.88027632G= , CM000673.1:g.88027632G=	GRCh37
NC_000011.8:g.87667280G=	NCBI36
NG_007952.1:g.48310C= , LRG_50:g.48310C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.934C= MANE Select	ENSP00000227266.4:p.Gln312=
ENST00000533897.2:n.5247C=
ENST00000676612.1:c.*741C=	ENSP00000504440.1:n.*741C=
ENST00000677208.1:c.*440C=	ENSP00000504347.1:n.*440C=
ENST00000677661.1:c.*611C=	ENSP00000503323.1:n.*611C=
ENST00000677802.1:c.*611C=	ENSP00000504115.1:n.*611C=
ENST00000678395.1:c.*440C=	ENSP00000503123.1:n.*440C=
ENST00000678464.1:c.901C=	ENSP00000503046.1:p.Gln301=
ENST00000678506.1:c.895C=	ENSP00000503580.1:p.Gln299=
ENST00000678520.1:c.*585C=	ENSP00000503361.1:n.*585C=
ENST00000678554.1:c.889+1669C=	ENSP00000504541.1:n.889+1669C=
ENST00000678915.1:c.802C=	ENSP00000504805.1:p.Gln268=
ENST00000679224.1:c.571C=	ENSP00000504475.1:p.Gln191=
ENST00000227266.9:c.934C=	ENSP00000227266.4:p.Gln312=
ENST00000533897.1:n.3668C=
NM_001814.4:c.934C= , LRG_50t1:c.934C=	NP_001805.3:p.Gln312=
NM_001814.5:c.934C=	NP_001805.3:p.Gln312=
NM_001814.6:c.934C= MANE Select	NP_001805.4:p.Gln312=