Canonical Allele Identifier: CA1989483578

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88296207C= , CM000673.2:g.88296207C=	GRCh38
NC_000011.9:g.88029375C= , CM000673.1:g.88029375C=	GRCh37
NC_000011.8:g.87669023C=	NCBI36
NG_007952.1:g.46567G= , LRG_50:g.46567G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.815G= MANE Select	NP_001805.4:p.Arg272=
ENST00000227266.10:c.815G= MANE Select	ENSP00000227266.4:p.Arg272=
NM_001814.4:c.815G= , LRG_50t1:c.815G=	NP_001805.3:p.Arg272=
NM_001814.5:c.815G=	NP_001805.3:p.Arg272=
ENST00000227266.9:c.815G=	ENSP00000227266.4:p.Arg272=
ENST00000527018.5:c.685G=
ENST00000527018.6:c.815G=	ENSP00000432556.2:p.Arg272=
ENST00000533897.1:n.3549G=
ENST00000533897.2:n.5128G=
ENST00000676612.1:c.*622G=	ENSP00000504440.1:n.*622G=
ENST00000677208.1:c.*321G=	ENSP00000504347.1:n.*321G=
ENST00000677661.1:c.*492G=	ENSP00000503323.1:n.*492G=
ENST00000677802.1:c.*492G=	ENSP00000504115.1:n.*492G=
ENST00000678395.1:c.*321G=	ENSP00000503123.1:n.*321G=
ENST00000678464.1:c.815G=	ENSP00000503046.1:p.Arg272=
ENST00000678506.1:c.776G=	ENSP00000503580.1:p.Arg259=
ENST00000678520.1:c.*466G=	ENSP00000503361.1:n.*466G=
ENST00000678554.1:c.815G=	ENSP00000504541.1:p.Arg272=
ENST00000678915.1:c.758-1699G=	ENSP00000504805.1:n.758-1699G=
ENST00000679224.1:c.452G=	ENSP00000504475.1:p.Arg151=