Canonical Allele Identifier: CA1989482780
Gene: CTSC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88294403T= , CM000673.2:g.88294403T= GRCh38
NC_000011.9:g.88027571T= , CM000673.1:g.88027571T= GRCh37
NC_000011.8:g.87667219T= NCBI36
NG_007952.1:g.48371A= , LRG_50:g.48371A=

Transcript Alleles

HGVS Amino-acid change
ENST00000227266.10:c.995A= MANE Select ENSP00000227266.4:p.Lys332=
ENST00000533897.2:n.5308A=
ENST00000676612.1:c.*802A= ENSP00000504440.1:n.*802A=
ENST00000677208.1:c.*501A= ENSP00000504347.1:n.*501A=
ENST00000677661.1:c.*672A= ENSP00000503323.1:n.*672A=
ENST00000677802.1:c.*672A= ENSP00000504115.1:n.*672A=
ENST00000678395.1:c.*501A= ENSP00000503123.1:n.*501A=
ENST00000678464.1:c.962A= ENSP00000503046.1:p.Lys321=
ENST00000678506.1:c.956A= ENSP00000503580.1:p.Lys319=
ENST00000678520.1:c.*646A= ENSP00000503361.1:n.*646A=
ENST00000678554.1:c.889+1730A= ENSP00000504541.1:n.889+1730A=
ENST00000678915.1:c.863A= ENSP00000504805.1:p.Lys288=
ENST00000679224.1:c.632A= ENSP00000504475.1:p.Lys211=
ENST00000227266.9:c.995A= ENSP00000227266.4:p.Lys332=
ENST00000533897.1:n.3729A=
NM_001814.4:c.995A= , LRG_50t1:c.995A= NP_001805.3:p.Lys332=
NM_001814.5:c.995A= NP_001805.3:p.Lys332=
NM_001814.6:c.995A= MANE Select NP_001805.4:p.Lys332=