Canonical Allele Identifier: CA382022134

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027581A>T (hg19) ; chr11:g.88294413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294413A>T , CM000673.2:g.88294413A>T	GRCh38
NC_000011.9:g.88027581A>T , CM000673.1:g.88027581A>T	GRCh37
NC_000011.8:g.87667229A>T	NCBI36
NG_007952.1:g.48361T>A , LRG_50:g.48361T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.985T>A MANE Select	ENSP00000227266.4:p.Ser329Thr
ENST00000533897.2:n.5298T>A
ENST00000676612.1:c.*792T>A	ENSP00000504440.1:n.*792T>A
ENST00000677208.1:c.*491T>A	ENSP00000504347.1:n.*491T>A
ENST00000677661.1:c.*662T>A	ENSP00000503323.1:n.*662T>A
ENST00000677802.1:c.*662T>A	ENSP00000504115.1:n.*662T>A
ENST00000678395.1:c.*491T>A	ENSP00000503123.1:n.*491T>A
ENST00000678464.1:c.952T>A	ENSP00000503046.1:p.Ser318Thr
ENST00000678506.1:c.946T>A	ENSP00000503580.1:p.Ser316Thr
ENST00000678520.1:c.*636T>A	ENSP00000503361.1:n.*636T>A
ENST00000678554.1:c.889+1720T>A	ENSP00000504541.1:n.889+1720T>A
ENST00000678915.1:c.853T>A	ENSP00000504805.1:p.Ser285Thr
ENST00000679224.1:c.622T>A	ENSP00000504475.1:p.Ser208Thr
ENST00000227266.9:c.985T>A	ENSP00000227266.4:p.Ser329Thr
ENST00000533897.1:n.3719T>A
NM_001814.4:c.985T>A , LRG_50t1:c.985T>A	NP_001805.3:p.Ser329Thr
NM_001814.5:c.985T>A	NP_001805.3:p.Ser329Thr
NM_001814.6:c.985T>A MANE Select	NP_001805.4:p.Ser329Thr