Canonical Allele Identifier: CA476145394

Gene: CTSC

Linked Data

• gnomAD v4: 11-88294348-A-G
• MyVariant Identifiers: chr11:g.88027516A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294348A>G , CM000673.2:g.88294348A>G	GRCh38
NC_000011.9:g.88027516A>G , CM000673.1:g.88027516A>G	GRCh37
NC_000011.8:g.87667164A>G	NCBI36
NG_007952.1:g.48426T>C , LRG_50:g.48426T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1050T>C MANE Select	ENSP00000227266.4:p.Gly350=
ENST00000533897.2:n.5363T>C
ENST00000676612.1:c.*857T>C	ENSP00000504440.1:n.*857T>C
ENST00000677208.1:c.*556T>C	ENSP00000504347.1:n.*556T>C
ENST00000677661.1:c.*727T>C	ENSP00000503323.1:n.*727T>C
ENST00000677802.1:c.*727T>C	ENSP00000504115.1:n.*727T>C
ENST00000678395.1:c.*556T>C	ENSP00000503123.1:n.*556T>C
ENST00000678464.1:c.1017T>C	ENSP00000503046.1:p.Gly339=
ENST00000678506.1:c.1011T>C	ENSP00000503580.1:p.Gly337=
ENST00000678520.1:c.*701T>C	ENSP00000503361.1:n.*701T>C
ENST00000678554.1:c.889+1785T>C	ENSP00000504541.1:n.889+1785T>C
ENST00000678915.1:c.918T>C	ENSP00000504805.1:p.Gly306=
ENST00000679224.1:c.687T>C	ENSP00000504475.1:p.Gly229=
ENST00000227266.9:c.1050T>C	ENSP00000227266.4:p.Gly350=
ENST00000533897.1:n.3784T>C
NM_001814.4:c.1050T>C , LRG_50t1:c.1050T>C	NP_001805.3:p.Gly350=
NM_001814.5:c.1050T>C	NP_001805.3:p.Gly350=
NM_001814.6:c.1050T>C MANE Select	NP_001805.4:p.Gly350=