Canonical Allele Identifier: CA1989482774

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294392C= , CM000673.2:g.88294392C=	GRCh38
NC_000011.9:g.88027560C= , CM000673.1:g.88027560C=	GRCh37
NC_000011.8:g.87667208C=	NCBI36
NG_007952.1:g.48382G= , LRG_50:g.48382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1006G= MANE Select	ENSP00000227266.4:p.Asp336=
ENST00000533897.2:n.5319G=
ENST00000676612.1:c.*813G=	ENSP00000504440.1:n.*813G=
ENST00000677208.1:c.*512G=	ENSP00000504347.1:n.*512G=
ENST00000677661.1:c.*683G=	ENSP00000503323.1:n.*683G=
ENST00000677802.1:c.*683G=	ENSP00000504115.1:n.*683G=
ENST00000678395.1:c.*512G=	ENSP00000503123.1:n.*512G=
ENST00000678464.1:c.973G=	ENSP00000503046.1:p.Asp325=
ENST00000678506.1:c.967G=	ENSP00000503580.1:p.Asp323=
ENST00000678520.1:c.*657G=	ENSP00000503361.1:n.*657G=
ENST00000678554.1:c.889+1741G=	ENSP00000504541.1:n.889+1741G=
ENST00000678915.1:c.874G=	ENSP00000504805.1:p.Asp292=
ENST00000679224.1:c.643G=	ENSP00000504475.1:p.Asp215=
ENST00000227266.9:c.1006G=	ENSP00000227266.4:p.Asp336=
ENST00000533897.1:n.3740G=
NM_001814.4:c.1006G= , LRG_50t1:c.1006G=	NP_001805.3:p.Asp336=
NM_001814.5:c.1006G=	NP_001805.3:p.Asp336=
NM_001814.6:c.1006G= MANE Select	NP_001805.4:p.Asp336=