Canonical Allele Identifier: CA382022252

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027634G>C (hg19) ; chr11:g.88294466G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294466G>C , CM000673.2:g.88294466G>C	GRCh38
NC_000011.9:g.88027634G>C , CM000673.1:g.88027634G>C	GRCh37
NC_000011.8:g.87667282G>C	NCBI36
NG_007952.1:g.48308C>G , LRG_50:g.48308C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.932C>G MANE Select	ENSP00000227266.4:p.Ala311Gly
ENST00000533897.2:n.5245C>G
ENST00000676612.1:c.*739C>G	ENSP00000504440.1:n.*739C>G
ENST00000677208.1:c.*438C>G	ENSP00000504347.1:n.*438C>G
ENST00000677661.1:c.*609C>G	ENSP00000503323.1:n.*609C>G
ENST00000677802.1:c.*609C>G	ENSP00000504115.1:n.*609C>G
ENST00000678395.1:c.*438C>G	ENSP00000503123.1:n.*438C>G
ENST00000678464.1:c.899C>G	ENSP00000503046.1:p.Ala300Gly
ENST00000678506.1:c.893C>G	ENSP00000503580.1:p.Ala298Gly
ENST00000678520.1:c.*583C>G	ENSP00000503361.1:n.*583C>G
ENST00000678554.1:c.889+1667C>G	ENSP00000504541.1:n.889+1667C>G
ENST00000678915.1:c.800C>G	ENSP00000504805.1:p.Ala267Gly
ENST00000679224.1:c.569C>G	ENSP00000504475.1:p.Ala190Gly
ENST00000227266.9:c.932C>G	ENSP00000227266.4:p.Ala311Gly
ENST00000533897.1:n.3666C>G
NM_001814.4:c.932C>G , LRG_50t1:c.932C>G	NP_001805.3:p.Ala311Gly
NM_001814.5:c.932C>G	NP_001805.3:p.Ala311Gly
NM_001814.6:c.932C>G MANE Select	NP_001805.4:p.Ala311Gly