Canonical Allele Identifier: CA476145221

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027606A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294438A>G , CM000673.2:g.88294438A>G	GRCh38
NC_000011.9:g.88027606A>G , CM000673.1:g.88027606A>G	GRCh37
NC_000011.8:g.87667254A>G	NCBI36
NG_007952.1:g.48336T>C , LRG_50:g.48336T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.960T>C MANE Select	ENSP00000227266.4:p.Ala320=
ENST00000533897.2:n.5273T>C
ENST00000676612.1:c.*767T>C	ENSP00000504440.1:n.*767T>C
ENST00000677208.1:c.*466T>C	ENSP00000504347.1:n.*466T>C
ENST00000677661.1:c.*637T>C	ENSP00000503323.1:n.*637T>C
ENST00000677802.1:c.*637T>C	ENSP00000504115.1:n.*637T>C
ENST00000678395.1:c.*466T>C	ENSP00000503123.1:n.*466T>C
ENST00000678464.1:c.927T>C	ENSP00000503046.1:p.Ala309=
ENST00000678506.1:c.921T>C	ENSP00000503580.1:p.Ala307=
ENST00000678520.1:c.*611T>C	ENSP00000503361.1:n.*611T>C
ENST00000678554.1:c.889+1695T>C	ENSP00000504541.1:n.889+1695T>C
ENST00000678915.1:c.828T>C	ENSP00000504805.1:p.Ala276=
ENST00000679224.1:c.597T>C	ENSP00000504475.1:p.Ala199=
ENST00000227266.9:c.960T>C	ENSP00000227266.4:p.Ala320=
ENST00000533897.1:n.3694T>C
NM_001814.4:c.960T>C , LRG_50t1:c.960T>C	NP_001805.3:p.Ala320=
NM_001814.5:c.960T>C	NP_001805.3:p.Ala320=
NM_001814.6:c.960T>C MANE Select	NP_001805.4:p.Ala320=