Canonical Allele Identifier: CA1989490949

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88312430T= , CM000673.2:g.88312430T=	GRCh38
NC_000011.9:g.88045598T= , CM000673.1:g.88045598T=	GRCh37
NC_000011.8:g.87685246T=	NCBI36
NG_007952.1:g.30344A= , LRG_50:g.30344A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.443A= MANE Select	ENSP00000227266.4:p.Asn148=
ENST00000527018.6:c.443A=	ENSP00000432556.2:p.Asn148=
ENST00000533897.2:n.491A=
ENST00000676612.1:c.*250A=	ENSP00000504440.1:n.*250A=
ENST00000677208.1:c.319-3112A=	ENSP00000504347.1:n.319-3112A=
ENST00000677661.1:c.*120A=	ENSP00000503323.1:n.*120A=
ENST00000677802.1:c.*120A=	ENSP00000504115.1:n.*120A=
ENST00000678395.1:c.423+20A=	ENSP00000503123.1:n.423+20A=
ENST00000678464.1:c.443A=	ENSP00000503046.1:p.Asn148=
ENST00000678506.1:c.443A=	ENSP00000503580.1:p.Asn148=
ENST00000678520.1:c.*250A=	ENSP00000503361.1:n.*250A=
ENST00000678554.1:c.443A=	ENSP00000504541.1:p.Asn148=
ENST00000678915.1:c.443A=	ENSP00000504805.1:p.Asn148=
ENST00000679224.1:c.80A=	ENSP00000504475.1:p.Asn27=
ENST00000227266.9:c.443A=	ENSP00000227266.4:p.Asn148=
ENST00000527018.5:c.313A=
ENST00000533865.5:n.465A=
NM_001814.4:c.443A= , LRG_50t1:c.443A=	NP_001805.3:p.Asn148=
NM_001814.5:c.443A=	NP_001805.3:p.Asn148=
NM_001814.6:c.443A= MANE Select	NP_001805.4:p.Asn148=