Canonical Allele Identifier: CA476145406

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027537A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294369A>G , CM000673.2:g.88294369A>G	GRCh38
NC_000011.9:g.88027537A>G , CM000673.1:g.88027537A>G	GRCh37
NC_000011.8:g.87667185A>G	NCBI36
NG_007952.1:g.48405T>C , LRG_50:g.48405T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1029T>C MANE Select	ENSP00000227266.4:p.Ser343=
ENST00000533897.2:n.5342T>C
ENST00000676612.1:c.*836T>C	ENSP00000504440.1:n.*836T>C
ENST00000677208.1:c.*535T>C	ENSP00000504347.1:n.*535T>C
ENST00000677661.1:c.*706T>C	ENSP00000503323.1:n.*706T>C
ENST00000677802.1:c.*706T>C	ENSP00000504115.1:n.*706T>C
ENST00000678395.1:c.*535T>C	ENSP00000503123.1:n.*535T>C
ENST00000678464.1:c.996T>C	ENSP00000503046.1:p.Ser332=
ENST00000678506.1:c.990T>C	ENSP00000503580.1:p.Ser330=
ENST00000678520.1:c.*680T>C	ENSP00000503361.1:n.*680T>C
ENST00000678554.1:c.889+1764T>C	ENSP00000504541.1:n.889+1764T>C
ENST00000678915.1:c.897T>C	ENSP00000504805.1:p.Ser299=
ENST00000679224.1:c.666T>C	ENSP00000504475.1:p.Ser222=
ENST00000227266.9:c.1029T>C	ENSP00000227266.4:p.Ser343=
ENST00000533897.1:n.3763T>C
NM_001814.4:c.1029T>C , LRG_50t1:c.1029T>C	NP_001805.3:p.Ser343=
NM_001814.5:c.1029T>C	NP_001805.3:p.Ser343=
NM_001814.6:c.1029T>C MANE Select	NP_001805.4:p.Ser343=