Canonical Allele Identifier: CA382026612

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88312472C>T , CM000673.2:g.88312472C>T	GRCh38
NC_000011.9:g.88045640C>T , CM000673.1:g.88045640C>T	GRCh37
NC_000011.8:g.87685288C>T	NCBI36
NG_007952.1:g.30302G>A , LRG_50:g.30302G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.401G>A MANE Select	NP_001805.4:p.Trp134Ter
ENST00000227266.10:c.401G>A MANE Select	ENSP00000227266.4:p.Trp134Ter
NM_001814.4:c.401G>A , LRG_50t1:c.401G>A	NP_001805.3:p.Trp134Ter
NM_001814.5:c.401G>A	NP_001805.3:p.Trp134Ter
ENST00000227266.9:c.401G>A	ENSP00000227266.4:p.Trp134Ter
ENST00000527018.5:c.271G>A
ENST00000527018.6:c.401G>A	ENSP00000432556.2:p.Trp134Ter
ENST00000533865.5:n.423G>A
ENST00000533897.2:n.449G>A
ENST00000676612.1:c.*208G>A	ENSP00000504440.1:n.*208G>A
ENST00000677208.1:c.319-3154G>A	ENSP00000504347.1:n.319-3154G>A
ENST00000677661.1:c.*78G>A	ENSP00000503323.1:n.*78G>A
ENST00000677802.1:c.*78G>A	ENSP00000504115.1:n.*78G>A
ENST00000678395.1:c.401G>A	ENSP00000503123.1:p.Trp134Ter
ENST00000678464.1:c.401G>A	ENSP00000503046.1:p.Trp134Ter
ENST00000678506.1:c.401G>A	ENSP00000503580.1:p.Trp134Ter
ENST00000678520.1:c.*208G>A	ENSP00000503361.1:n.*208G>A
ENST00000678554.1:c.401G>A	ENSP00000504541.1:p.Trp134Ter
ENST00000678915.1:c.401G>A	ENSP00000504805.1:p.Trp134Ter
ENST00000679224.1:c.38G>A	ENSP00000504475.1:p.Trp13Ter