Canonical Allele Identifier: CA475929613

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88045585G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88312417G>A , CM000673.2:g.88312417G>A	GRCh38
NC_000011.9:g.88045585G>A , CM000673.1:g.88045585G>A	GRCh37
NC_000011.8:g.87685233G>A	NCBI36
NG_007952.1:g.30357C>T , LRG_50:g.30357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.456C>T MANE Select	ENSP00000227266.4:p.Asn152=
ENST00000527018.6:c.456C>T	ENSP00000432556.2:p.Asn152=
ENST00000533897.2:n.504C>T
ENST00000676612.1:c.*263C>T	ENSP00000504440.1:n.*263C>T
ENST00000677208.1:c.319-3099C>T	ENSP00000504347.1:n.319-3099C>T
ENST00000677661.1:c.*133C>T	ENSP00000503323.1:n.*133C>T
ENST00000677802.1:c.*133C>T	ENSP00000504115.1:n.*133C>T
ENST00000678395.1:c.423+33C>T	ENSP00000503123.1:n.423+33C>T
ENST00000678464.1:c.456C>T	ENSP00000503046.1:p.Asn152=
ENST00000678506.1:c.446+10C>T	ENSP00000503580.1:n.446+10C>T
ENST00000678520.1:c.*263C>T	ENSP00000503361.1:n.*263C>T
ENST00000678554.1:c.456C>T	ENSP00000504541.1:p.Asn152=
ENST00000678915.1:c.456C>T	ENSP00000504805.1:p.Asn152=
ENST00000679224.1:c.93C>T	ENSP00000504475.1:p.Asn31=
ENST00000227266.9:c.456C>T	ENSP00000227266.4:p.Asn152=
ENST00000527018.5:c.326C>T
ENST00000533865.5:n.478C>T
NM_001814.4:c.456C>T , LRG_50t1:c.456C>T	NP_001805.3:p.Asn152=
NM_001814.5:c.456C>T	NP_001805.3:p.Asn152=
NM_001814.6:c.456C>T MANE Select	NP_001805.4:p.Asn152=