Canonical Allele Identifier: CA382022285

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294481A>G , CM000673.2:g.88294481A>G	GRCh38
NC_000011.9:g.88027649A>G , CM000673.1:g.88027649A>G	GRCh37
NC_000011.8:g.87667297A>G	NCBI36
NG_007952.1:g.48293T>C , LRG_50:g.48293T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.917T>C MANE Select	NP_001805.4:p.Ile306Thr
ENST00000227266.10:c.917T>C MANE Select	ENSP00000227266.4:p.Ile306Thr
NM_001814.4:c.917T>C , LRG_50t1:c.917T>C	NP_001805.3:p.Ile306Thr
NM_001814.5:c.917T>C	NP_001805.3:p.Ile306Thr
ENST00000227266.9:c.917T>C	ENSP00000227266.4:p.Ile306Thr
ENST00000533897.1:n.3651T>C
ENST00000533897.2:n.5230T>C
ENST00000676612.1:c.*724T>C	ENSP00000504440.1:n.*724T>C
ENST00000677208.1:c.*423T>C	ENSP00000504347.1:n.*423T>C
ENST00000677661.1:c.*594T>C	ENSP00000503323.1:n.*594T>C
ENST00000677802.1:c.*594T>C	ENSP00000504115.1:n.*594T>C
ENST00000678395.1:c.*423T>C	ENSP00000503123.1:n.*423T>C
ENST00000678464.1:c.890-6T>C	ENSP00000503046.1:n.890-6T>C
ENST00000678506.1:c.878T>C	ENSP00000503580.1:p.Ile293Thr
ENST00000678520.1:c.*568T>C	ENSP00000503361.1:n.*568T>C
ENST00000678554.1:c.889+1652T>C	ENSP00000504541.1:n.889+1652T>C
ENST00000678915.1:c.785T>C	ENSP00000504805.1:p.Ile262Thr
ENST00000679224.1:c.554T>C	ENSP00000504475.1:p.Ile185Thr