Canonical Allele Identifier: CA382021989

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027517C>T (hg19) ; chr11:g.88294349C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294349C>T , CM000673.2:g.88294349C>T	GRCh38
NC_000011.9:g.88027517C>T , CM000673.1:g.88027517C>T	GRCh37
NC_000011.8:g.87667165C>T	NCBI36
NG_007952.1:g.48425G>A , LRG_50:g.48425G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1049G>A MANE Select	ENSP00000227266.4:p.Gly350Asp
ENST00000533897.2:n.5362G>A
ENST00000676612.1:c.*856G>A	ENSP00000504440.1:n.*856G>A
ENST00000677208.1:c.*555G>A	ENSP00000504347.1:n.*555G>A
ENST00000677661.1:c.*726G>A	ENSP00000503323.1:n.*726G>A
ENST00000677802.1:c.*726G>A	ENSP00000504115.1:n.*726G>A
ENST00000678395.1:c.*555G>A	ENSP00000503123.1:n.*555G>A
ENST00000678464.1:c.1016G>A	ENSP00000503046.1:p.Gly339Asp
ENST00000678506.1:c.1010G>A	ENSP00000503580.1:p.Gly337Asp
ENST00000678520.1:c.*700G>A	ENSP00000503361.1:n.*700G>A
ENST00000678554.1:c.889+1784G>A	ENSP00000504541.1:n.889+1784G>A
ENST00000678915.1:c.917G>A	ENSP00000504805.1:p.Gly306Asp
ENST00000679224.1:c.686G>A	ENSP00000504475.1:p.Gly229Asp
ENST00000227266.9:c.1049G>A	ENSP00000227266.4:p.Gly350Asp
ENST00000533897.1:n.3783G>A
NM_001814.4:c.1049G>A , LRG_50t1:c.1049G>A	NP_001805.3:p.Gly350Asp
NM_001814.5:c.1049G>A	NP_001805.3:p.Gly350Asp
NM_001814.6:c.1049G>A MANE Select	NP_001805.4:p.Gly350Asp