Canonical Allele Identifier: CA382022326

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027670T>A (hg19) ; chr11:g.88294502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294502T>A , CM000673.2:g.88294502T>A	GRCh38
NC_000011.9:g.88027670T>A , CM000673.1:g.88027670T>A	GRCh37
NC_000011.8:g.87667318T>A	NCBI36
NG_007952.1:g.48272A>T , LRG_50:g.48272A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.896A>T MANE Select	ENSP00000227266.4:p.Glu299Val
ENST00000533897.2:n.5209A>T
ENST00000676612.1:c.*703A>T	ENSP00000504440.1:n.*703A>T
ENST00000677208.1:c.*402A>T	ENSP00000504347.1:n.*402A>T
ENST00000677661.1:c.*573A>T	ENSP00000503323.1:n.*573A>T
ENST00000677802.1:c.*573A>T	ENSP00000504115.1:n.*573A>T
ENST00000678395.1:c.*402A>T	ENSP00000503123.1:n.*402A>T
ENST00000678464.1:c.890-27A>T	ENSP00000503046.1:n.890-27A>T
ENST00000678506.1:c.857A>T	ENSP00000503580.1:p.Glu286Val
ENST00000678520.1:c.*547A>T	ENSP00000503361.1:n.*547A>T
ENST00000678554.1:c.889+1631A>T	ENSP00000504541.1:n.889+1631A>T
ENST00000678915.1:c.764A>T	ENSP00000504805.1:p.Glu255Val
ENST00000679224.1:c.533A>T	ENSP00000504475.1:p.Glu178Val
ENST00000227266.9:c.896A>T	ENSP00000227266.4:p.Glu299Val
ENST00000533897.1:n.3630A>T
NM_001814.4:c.896A>T , LRG_50t1:c.896A>T	NP_001805.3:p.Glu299Val
NM_001814.5:c.896A>T	NP_001805.3:p.Glu299Val
NM_001814.6:c.896A>T MANE Select	NP_001805.4:p.Glu299Val