Canonical Allele Identifier: CA382022126

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027577G>C (hg19) ; chr11:g.88294409G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294409G>C , CM000673.2:g.88294409G>C	GRCh38
NC_000011.9:g.88027577G>C , CM000673.1:g.88027577G>C	GRCh37
NC_000011.8:g.87667225G>C	NCBI36
NG_007952.1:g.48365C>G , LRG_50:g.48365C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.989C>G MANE Select	ENSP00000227266.4:p.Pro330Arg
ENST00000533897.2:n.5302C>G
ENST00000676612.1:c.*796C>G	ENSP00000504440.1:n.*796C>G
ENST00000677208.1:c.*495C>G	ENSP00000504347.1:n.*495C>G
ENST00000677661.1:c.*666C>G	ENSP00000503323.1:n.*666C>G
ENST00000677802.1:c.*666C>G	ENSP00000504115.1:n.*666C>G
ENST00000678395.1:c.*495C>G	ENSP00000503123.1:n.*495C>G
ENST00000678464.1:c.956C>G	ENSP00000503046.1:p.Pro319Arg
ENST00000678506.1:c.950C>G	ENSP00000503580.1:p.Pro317Arg
ENST00000678520.1:c.*640C>G	ENSP00000503361.1:n.*640C>G
ENST00000678554.1:c.889+1724C>G	ENSP00000504541.1:n.889+1724C>G
ENST00000678915.1:c.857C>G	ENSP00000504805.1:p.Pro286Arg
ENST00000679224.1:c.626C>G	ENSP00000504475.1:p.Pro209Arg
ENST00000227266.9:c.989C>G	ENSP00000227266.4:p.Pro330Arg
ENST00000533897.1:n.3723C>G
NM_001814.4:c.989C>G , LRG_50t1:c.989C>G	NP_001805.3:p.Pro330Arg
NM_001814.5:c.989C>G	NP_001805.3:p.Pro330Arg
NM_001814.6:c.989C>G MANE Select	NP_001805.4:p.Pro330Arg