Canonical Allele Identifier: CA382022351

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88296132C>T , CM000673.2:g.88296132C>T	GRCh38
NC_000011.9:g.88029300C>T , CM000673.1:g.88029300C>T	GRCh37
NC_000011.8:g.87668948C>T	NCBI36
NG_007952.1:g.46642G>A , LRG_50:g.46642G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.889+1G>A MANE Select	NP_001805.4:n.889+1G>A
ENST00000227266.10:c.889+1G>A MANE Select	ENSP00000227266.4:n.889+1G>A
NM_001814.4:c.889+1G>A , LRG_50t1:c.889+1G>A	NP_001805.3:n.889+1G>A
NM_001814.5:c.889+1G>A	NP_001805.3:n.889+1G>A
ENST00000227266.9:c.889+1G>A	ENSP00000227266.4:n.889+1G>A
ENST00000527018.6:c.890G>A	ENSP00000432556.2:p.Gly297Asp
ENST00000533897.1:n.3623+1G>A
ENST00000533897.2:n.5202+1G>A
ENST00000676612.1:c.*696+1G>A	ENSP00000504440.1:n.*696+1G>A
ENST00000677208.1:c.*395+1G>A	ENSP00000504347.1:n.*395+1G>A
ENST00000677661.1:c.*566+1G>A	ENSP00000503323.1:n.*566+1G>A
ENST00000677802.1:c.*566+1G>A	ENSP00000504115.1:n.*566+1G>A
ENST00000678395.1:c.*395+1G>A	ENSP00000503123.1:n.*395+1G>A
ENST00000678464.1:c.889+1G>A	ENSP00000503046.1:n.889+1G>A
ENST00000678506.1:c.850+1G>A	ENSP00000503580.1:n.850+1G>A
ENST00000678520.1:c.*540+1G>A	ENSP00000503361.1:n.*540+1G>A
ENST00000678554.1:c.889+1G>A	ENSP00000504541.1:n.889+1G>A
ENST00000678915.1:c.758-1624G>A	ENSP00000504805.1:n.758-1624G>A
ENST00000679224.1:c.526+1G>A	ENSP00000504475.1:n.526+1G>A