Canonical Allele Identifier: CA1989482814

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294497C= , CM000673.2:g.88294497C=	GRCh38
NC_000011.9:g.88027665C= , CM000673.1:g.88027665C=	GRCh37
NC_000011.8:g.87667313C=	NCBI36
NG_007952.1:g.48277G= , LRG_50:g.48277G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.901G= MANE Select	NP_001805.4:p.Gly301=
ENST00000227266.10:c.901G= MANE Select	ENSP00000227266.4:p.Gly301=
NM_001814.4:c.901G= , LRG_50t1:c.901G=	NP_001805.3:p.Gly301=
NM_001814.5:c.901G=	NP_001805.3:p.Gly301=
ENST00000227266.9:c.901G=	ENSP00000227266.4:p.Gly301=
ENST00000533897.1:n.3635G=
ENST00000533897.2:n.5214G=
ENST00000676612.1:c.*708G=	ENSP00000504440.1:n.*708G=
ENST00000677208.1:c.*407G=	ENSP00000504347.1:n.*407G=
ENST00000677661.1:c.*578G=	ENSP00000503323.1:n.*578G=
ENST00000677802.1:c.*578G=	ENSP00000504115.1:n.*578G=
ENST00000678395.1:c.*407G=	ENSP00000503123.1:n.*407G=
ENST00000678464.1:c.890-22G=	ENSP00000503046.1:n.890-22G=
ENST00000678506.1:c.862G=	ENSP00000503580.1:p.Gly288=
ENST00000678520.1:c.*552G=	ENSP00000503361.1:n.*552G=
ENST00000678554.1:c.889+1636G=	ENSP00000504541.1:n.889+1636G=
ENST00000678915.1:c.769G=	ENSP00000504805.1:p.Gly257=
ENST00000679224.1:c.538G=	ENSP00000504475.1:p.Gly180=