Canonical Allele Identifier: CA1989482750

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294349C= , CM000673.2:g.88294349C=	GRCh38
NC_000011.9:g.88027517C= , CM000673.1:g.88027517C=	GRCh37
NC_000011.8:g.87667165C=	NCBI36
NG_007952.1:g.48425G= , LRG_50:g.48425G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1049G= MANE Select	ENSP00000227266.4:p.Gly350=
ENST00000533897.2:n.5362G=
ENST00000676612.1:c.*856G=	ENSP00000504440.1:n.*856G=
ENST00000677208.1:c.*555G=	ENSP00000504347.1:n.*555G=
ENST00000677661.1:c.*726G=	ENSP00000503323.1:n.*726G=
ENST00000677802.1:c.*726G=	ENSP00000504115.1:n.*726G=
ENST00000678395.1:c.*555G=	ENSP00000503123.1:n.*555G=
ENST00000678464.1:c.1016G=	ENSP00000503046.1:p.Gly339=
ENST00000678506.1:c.1010G=	ENSP00000503580.1:p.Gly337=
ENST00000678520.1:c.*700G=	ENSP00000503361.1:n.*700G=
ENST00000678554.1:c.889+1784G=	ENSP00000504541.1:n.889+1784G=
ENST00000678915.1:c.917G=	ENSP00000504805.1:p.Gly306=
ENST00000679224.1:c.686G=	ENSP00000504475.1:p.Gly229=
ENST00000227266.9:c.1049G=	ENSP00000227266.4:p.Gly350=
ENST00000533897.1:n.3783G=
NM_001814.4:c.1049G= , LRG_50t1:c.1049G=	NP_001805.3:p.Gly350=
NM_001814.5:c.1049G=	NP_001805.3:p.Gly350=
NM_001814.6:c.1049G= MANE Select	NP_001805.4:p.Gly350=