Canonical Allele Identifier: CA476145403

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027531G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294363G>A , CM000673.2:g.88294363G>A	GRCh38
NC_000011.9:g.88027531G>A , CM000673.1:g.88027531G>A	GRCh37
NC_000011.8:g.87667179G>A	NCBI36
NG_007952.1:g.48411C>T , LRG_50:g.48411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1035C>T MANE Select	ENSP00000227266.4:p.Tyr345=
ENST00000533897.2:n.5348C>T
ENST00000676612.1:c.*842C>T	ENSP00000504440.1:n.*842C>T
ENST00000677208.1:c.*541C>T	ENSP00000504347.1:n.*541C>T
ENST00000677661.1:c.*712C>T	ENSP00000503323.1:n.*712C>T
ENST00000677802.1:c.*712C>T	ENSP00000504115.1:n.*712C>T
ENST00000678395.1:c.*541C>T	ENSP00000503123.1:n.*541C>T
ENST00000678464.1:c.1002C>T	ENSP00000503046.1:p.Tyr334=
ENST00000678506.1:c.996C>T	ENSP00000503580.1:p.Tyr332=
ENST00000678520.1:c.*686C>T	ENSP00000503361.1:n.*686C>T
ENST00000678554.1:c.889+1770C>T	ENSP00000504541.1:n.889+1770C>T
ENST00000678915.1:c.903C>T	ENSP00000504805.1:p.Tyr301=
ENST00000679224.1:c.672C>T	ENSP00000504475.1:p.Tyr224=
ENST00000227266.9:c.1035C>T	ENSP00000227266.4:p.Tyr345=
ENST00000533897.1:n.3769C>T
NM_001814.4:c.1035C>T , LRG_50t1:c.1035C>T	NP_001805.3:p.Tyr345=
NM_001814.5:c.1035C>T	NP_001805.3:p.Tyr345=
NM_001814.6:c.1035C>T MANE Select	NP_001805.4:p.Tyr345=