Canonical Allele Identifier: CA476145233

Gene: CTSC

Linked Data

• gnomAD v4: 11-88294453-C-T
• MyVariant Identifiers: chr11:g.88027621C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294453C>T , CM000673.2:g.88294453C>T	GRCh38
NC_000011.9:g.88027621C>T , CM000673.1:g.88027621C>T	GRCh37
NC_000011.8:g.87667269C>T	NCBI36
NG_007952.1:g.48321G>A , LRG_50:g.48321G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.945G>A MANE Select	ENSP00000227266.4:p.Gly315=
ENST00000533897.2:n.5258G>A
ENST00000676612.1:c.*752G>A	ENSP00000504440.1:n.*752G>A
ENST00000677208.1:c.*451G>A	ENSP00000504347.1:n.*451G>A
ENST00000677661.1:c.*622G>A	ENSP00000503323.1:n.*622G>A
ENST00000677802.1:c.*622G>A	ENSP00000504115.1:n.*622G>A
ENST00000678395.1:c.*451G>A	ENSP00000503123.1:n.*451G>A
ENST00000678464.1:c.912G>A	ENSP00000503046.1:p.Gly304=
ENST00000678506.1:c.906G>A	ENSP00000503580.1:p.Gly302=
ENST00000678520.1:c.*596G>A	ENSP00000503361.1:n.*596G>A
ENST00000678554.1:c.889+1680G>A	ENSP00000504541.1:n.889+1680G>A
ENST00000678915.1:c.813G>A	ENSP00000504805.1:p.Gly271=
ENST00000679224.1:c.582G>A	ENSP00000504475.1:p.Gly194=
ENST00000227266.9:c.945G>A	ENSP00000227266.4:p.Gly315=
ENST00000533897.1:n.3679G>A
NM_001814.4:c.945G>A , LRG_50t1:c.945G>A	NP_001805.3:p.Gly315=
NM_001814.5:c.945G>A	NP_001805.3:p.Gly315=
NM_001814.6:c.945G>A MANE Select	NP_001805.4:p.Gly315=