Canonical Allele Identifier: CA1989489458

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88309184C= , CM000673.2:g.88309184C=	GRCh38
NC_000011.9:g.88042352C= , CM000673.1:g.88042352C=	GRCh37
NC_000011.8:g.87682000C=	NCBI36
NG_007952.1:g.33590G= , LRG_50:g.33590G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.620G= MANE Select	ENSP00000227266.4:p.Gly207=
ENST00000527018.6:c.620G=	ENSP00000432556.2:p.Gly207=
ENST00000533897.2:n.668G=
ENST00000676612.1:c.*427G=	ENSP00000504440.1:n.*427G=
ENST00000677208.1:c.*126G=	ENSP00000504347.1:n.*126G=
ENST00000677661.1:c.*297G=	ENSP00000503323.1:n.*297G=
ENST00000677802.1:c.*297G=	ENSP00000504115.1:n.*297G=
ENST00000678065.1:n.180G=
ENST00000678395.1:c.*126G=	ENSP00000503123.1:n.*126G=
ENST00000678464.1:c.620G=	ENSP00000503046.1:p.Gly207=
ENST00000678506.1:c.581G=	ENSP00000503580.1:p.Gly194=
ENST00000678520.1:c.*292+3204G=	ENSP00000503361.1:n.*292+3204G=
ENST00000678554.1:c.620G=	ENSP00000504541.1:p.Gly207=
ENST00000678915.1:c.620G=	ENSP00000504805.1:p.Gly207=
ENST00000679224.1:c.257G=	ENSP00000504475.1:p.Gly86=
ENST00000227266.9:c.620G=	ENSP00000227266.4:p.Gly207=
ENST00000527018.5:c.490G=
NM_001814.4:c.620G= , LRG_50t1:c.620G=	NP_001805.3:p.Gly207=
NM_001814.5:c.620G=	NP_001805.3:p.Gly207=
NM_001814.6:c.620G= MANE Select	NP_001805.4:p.Gly207=