Canonical Allele Identifier: CA476145285

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294159G>A , CM000673.2:g.88294159G>A	GRCh38
NC_000011.9:g.88027327G>A , CM000673.1:g.88027327G>A	GRCh37
NC_000011.8:g.87666975G>A	NCBI36
NG_007952.1:g.48615C>T , LRG_50:g.48615C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.1239C>T MANE Select	NP_001805.4:p.Gly413=
ENST00000227266.10:c.1239C>T MANE Select	ENSP00000227266.4:p.Gly413=
NM_001814.4:c.1239C>T , LRG_50t1:c.1239C>T	NP_001805.3:p.Gly413=
NM_001814.5:c.1239C>T	NP_001805.3:p.Gly413=
ENST00000227266.9:c.1239C>T	ENSP00000227266.4:p.Gly413=
ENST00000533897.1:n.3973C>T
ENST00000533897.2:n.5552C>T
ENST00000676612.1:c.*1046C>T	ENSP00000504440.1:n.*1046C>T
ENST00000677208.1:c.*745C>T	ENSP00000504347.1:n.*745C>T
ENST00000677661.1:c.*916C>T	ENSP00000503323.1:n.*916C>T
ENST00000677802.1:c.*916C>T	ENSP00000504115.1:n.*916C>T
ENST00000678395.1:c.*745C>T	ENSP00000503123.1:n.*745C>T
ENST00000678464.1:c.1206C>T	ENSP00000503046.1:p.Gly402=
ENST00000678506.1:c.1200C>T	ENSP00000503580.1:p.Gly400=
ENST00000678520.1:c.*890C>T	ENSP00000503361.1:n.*890C>T
ENST00000678554.1:c.889+1974C>T	ENSP00000504541.1:n.889+1974C>T
ENST00000678915.1:c.1107C>T	ENSP00000504805.1:p.Gly369=
ENST00000679224.1:c.876C>T	ENSP00000504475.1:p.Gly292=