Canonical Allele Identifier: CA1989490946

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88312426C= , CM000673.2:g.88312426C=	GRCh38
NC_000011.9:g.88045594C= , CM000673.1:g.88045594C=	GRCh37
NC_000011.8:g.87685242C=	NCBI36
NG_007952.1:g.30348G= , LRG_50:g.30348G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.447G= MANE Select	ENSP00000227266.4:p.Val149=
ENST00000527018.6:c.447G=	ENSP00000432556.2:p.Val149=
ENST00000533897.2:n.495G=
ENST00000676612.1:c.*254G=	ENSP00000504440.1:n.*254G=
ENST00000677208.1:c.319-3108G=	ENSP00000504347.1:n.319-3108G=
ENST00000677661.1:c.*124G=	ENSP00000503323.1:n.*124G=
ENST00000677802.1:c.*124G=	ENSP00000504115.1:n.*124G=
ENST00000678395.1:c.423+24G=	ENSP00000503123.1:n.423+24G=
ENST00000678464.1:c.447G=	ENSP00000503046.1:p.Val149=
ENST00000678506.1:c.446+1G=	ENSP00000503580.1:n.446+1G=
ENST00000678520.1:c.*254G=	ENSP00000503361.1:n.*254G=
ENST00000678554.1:c.447G=	ENSP00000504541.1:p.Val149=
ENST00000678915.1:c.447G=	ENSP00000504805.1:p.Val149=
ENST00000679224.1:c.84G=	ENSP00000504475.1:p.Val28=
ENST00000227266.9:c.447G=	ENSP00000227266.4:p.Val149=
ENST00000527018.5:c.317G=
ENST00000533865.5:n.469G=
NM_001814.4:c.447G= , LRG_50t1:c.447G=	NP_001805.3:p.Val149=
NM_001814.5:c.447G=	NP_001805.3:p.Val149=
NM_001814.6:c.447G= MANE Select	NP_001805.4:p.Val149=