Canonical Allele Identifier: CA382021925

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027488T>G (hg19) ; chr11:g.88294320T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294320T>G , CM000673.2:g.88294320T>G	GRCh38
NC_000011.9:g.88027488T>G , CM000673.1:g.88027488T>G	GRCh37
NC_000011.8:g.87667136T>G	NCBI36
NG_007952.1:g.48454A>C , LRG_50:g.48454A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1078A>C MANE Select	ENSP00000227266.4:p.Met360Leu
ENST00000533897.2:n.5391A>C
ENST00000676612.1:c.*885A>C	ENSP00000504440.1:n.*885A>C
ENST00000677208.1:c.*584A>C	ENSP00000504347.1:n.*584A>C
ENST00000677661.1:c.*755A>C	ENSP00000503323.1:n.*755A>C
ENST00000677802.1:c.*755A>C	ENSP00000504115.1:n.*755A>C
ENST00000678395.1:c.*584A>C	ENSP00000503123.1:n.*584A>C
ENST00000678464.1:c.1045A>C	ENSP00000503046.1:p.Met349Leu
ENST00000678506.1:c.1039A>C	ENSP00000503580.1:p.Met347Leu
ENST00000678520.1:c.*729A>C	ENSP00000503361.1:n.*729A>C
ENST00000678554.1:c.889+1813A>C	ENSP00000504541.1:n.889+1813A>C
ENST00000678915.1:c.946A>C	ENSP00000504805.1:p.Met316Leu
ENST00000679224.1:c.715A>C	ENSP00000504475.1:p.Met239Leu
ENST00000227266.9:c.1078A>C	ENSP00000227266.4:p.Met360Leu
ENST00000533897.1:n.3812A>C
NM_001814.4:c.1078A>C , LRG_50t1:c.1078A>C	NP_001805.3:p.Met360Leu
NM_001814.5:c.1078A>C	NP_001805.3:p.Met360Leu
NM_001814.6:c.1078A>C MANE Select	NP_001805.4:p.Met360Leu