Canonical Allele Identifier: CA1989482784

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294418G= , CM000673.2:g.88294418G=	GRCh38
NC_000011.9:g.88027586G= , CM000673.1:g.88027586G=	GRCh37
NC_000011.8:g.87667234G=	NCBI36
NG_007952.1:g.48356C= , LRG_50:g.48356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.980C= MANE Select	ENSP00000227266.4:p.Thr327=
ENST00000533897.2:n.5293C=
ENST00000676612.1:c.*787C=	ENSP00000504440.1:n.*787C=
ENST00000677208.1:c.*486C=	ENSP00000504347.1:n.*486C=
ENST00000677661.1:c.*657C=	ENSP00000503323.1:n.*657C=
ENST00000677802.1:c.*657C=	ENSP00000504115.1:n.*657C=
ENST00000678395.1:c.*486C=	ENSP00000503123.1:n.*486C=
ENST00000678464.1:c.947C=	ENSP00000503046.1:p.Thr316=
ENST00000678506.1:c.941C=	ENSP00000503580.1:p.Thr314=
ENST00000678520.1:c.*631C=	ENSP00000503361.1:n.*631C=
ENST00000678554.1:c.889+1715C=	ENSP00000504541.1:n.889+1715C=
ENST00000678915.1:c.848C=	ENSP00000504805.1:p.Thr283=
ENST00000679224.1:c.617C=	ENSP00000504475.1:p.Thr206=
ENST00000227266.9:c.980C=	ENSP00000227266.4:p.Thr327=
ENST00000533897.1:n.3714C=
NM_001814.4:c.980C= , LRG_50t1:c.980C=	NP_001805.3:p.Thr327=
NM_001814.5:c.980C=	NP_001805.3:p.Thr327=
NM_001814.6:c.980C= MANE Select	NP_001805.4:p.Thr327=