Canonical Allele Identifier: CA225416951

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294112C>T , CM000673.2:g.88294112C>T	GRCh38
NC_000011.9:g.88027280C>T , CM000673.1:g.88027280C>T	GRCh37
NC_000011.8:g.87666928C>T	NCBI36
NG_007952.1:g.48662G>A , LRG_50:g.48662G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.1286G>A MANE Select	NP_001805.4:p.Trp429Ter
ENST00000227266.10:c.1286G>A MANE Select	ENSP00000227266.4:p.Trp429Ter
NM_001814.4:c.1286G>A , LRG_50t1:c.1286G>A	NP_001805.3:p.Trp429Ter
NM_001814.5:c.1286G>A	NP_001805.3:p.Trp429Ter
ENST00000227266.9:c.1286G>A	ENSP00000227266.4:p.Trp429Ter
ENST00000533897.1:n.4020G>A
ENST00000533897.2:n.5599G>A
ENST00000676612.1:c.*1093G>A	ENSP00000504440.1:n.*1093G>A
ENST00000677208.1:c.*792G>A	ENSP00000504347.1:n.*792G>A
ENST00000677661.1:c.*963G>A	ENSP00000503323.1:n.*963G>A
ENST00000677802.1:c.*963G>A	ENSP00000504115.1:n.*963G>A
ENST00000678395.1:c.*792G>A	ENSP00000503123.1:n.*792G>A
ENST00000678464.1:c.1253G>A	ENSP00000503046.1:p.Trp418Ter
ENST00000678506.1:c.1247G>A	ENSP00000503580.1:p.Trp416Ter
ENST00000678520.1:c.*937G>A	ENSP00000503361.1:n.*937G>A
ENST00000678554.1:c.889+2021G>A	ENSP00000504541.1:n.889+2021G>A
ENST00000678915.1:c.1154G>A	ENSP00000504805.1:p.Trp385Ter
ENST00000679224.1:c.923G>A	ENSP00000504475.1:p.Trp308Ter