Canonical Allele Identifier: CA382022261

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027638A>C (hg19) ; chr11:g.88294470A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294470A>C , CM000673.2:g.88294470A>C	GRCh38
NC_000011.9:g.88027638A>C , CM000673.1:g.88027638A>C	GRCh37
NC_000011.8:g.87667286A>C	NCBI36
NG_007952.1:g.48304T>G , LRG_50:g.48304T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.928T>G MANE Select	ENSP00000227266.4:p.Tyr310Asp
ENST00000533897.2:n.5241T>G
ENST00000676612.1:c.*735T>G	ENSP00000504440.1:n.*735T>G
ENST00000677208.1:c.*434T>G	ENSP00000504347.1:n.*434T>G
ENST00000677661.1:c.*605T>G	ENSP00000503323.1:n.*605T>G
ENST00000677802.1:c.*605T>G	ENSP00000504115.1:n.*605T>G
ENST00000678395.1:c.*434T>G	ENSP00000503123.1:n.*434T>G
ENST00000678464.1:c.895T>G	ENSP00000503046.1:p.Tyr299Asp
ENST00000678506.1:c.889T>G	ENSP00000503580.1:p.Tyr297Asp
ENST00000678520.1:c.*579T>G	ENSP00000503361.1:n.*579T>G
ENST00000678554.1:c.889+1663T>G	ENSP00000504541.1:n.889+1663T>G
ENST00000678915.1:c.796T>G	ENSP00000504805.1:p.Tyr266Asp
ENST00000679224.1:c.565T>G	ENSP00000504475.1:p.Tyr189Asp
ENST00000227266.9:c.928T>G	ENSP00000227266.4:p.Tyr310Asp
ENST00000533897.1:n.3662T>G
NM_001814.4:c.928T>G , LRG_50t1:c.928T>G	NP_001805.3:p.Tyr310Asp
NM_001814.5:c.928T>G	NP_001805.3:p.Tyr310Asp
NM_001814.6:c.928T>G MANE Select	NP_001805.4:p.Tyr310Asp