Canonical Allele Identifier: CA6219780

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294331T>C , CM000673.2:g.88294331T>C	GRCh38
NC_000011.9:g.88027499T>C , CM000673.1:g.88027499T>C	GRCh37
NC_000011.8:g.87667147T>C	NCBI36
NG_007952.1:g.48443A>G , LRG_50:g.48443A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.1067A>G MANE Select	NP_001805.4:p.Asn356Ser
ENST00000227266.10:c.1067A>G MANE Select	ENSP00000227266.4:p.Asn356Ser
NM_001814.4:c.1067A>G , LRG_50t1:c.1067A>G	NP_001805.3:p.Asn356Ser
NM_001814.5:c.1067A>G	NP_001805.3:p.Asn356Ser
ENST00000227266.9:c.1067A>G	ENSP00000227266.4:p.Asn356Ser
ENST00000533897.1:n.3801A>G
ENST00000533897.2:n.5380A>G
ENST00000676612.1:c.*874A>G	ENSP00000504440.1:n.*874A>G
ENST00000677208.1:c.*573A>G	ENSP00000504347.1:n.*573A>G
ENST00000677661.1:c.*744A>G	ENSP00000503323.1:n.*744A>G
ENST00000677802.1:c.*744A>G	ENSP00000504115.1:n.*744A>G
ENST00000678395.1:c.*573A>G	ENSP00000503123.1:n.*573A>G
ENST00000678464.1:c.1034A>G	ENSP00000503046.1:p.Asn345Ser
ENST00000678506.1:c.1028A>G	ENSP00000503580.1:p.Asn343Ser
ENST00000678520.1:c.*718A>G	ENSP00000503361.1:n.*718A>G
ENST00000678554.1:c.889+1802A>G	ENSP00000504541.1:n.889+1802A>G
ENST00000678915.1:c.935A>G	ENSP00000504805.1:p.Asn312Ser
ENST00000679224.1:c.704A>G	ENSP00000504475.1:p.Asn235Ser