Canonical Allele Identifier: CA476145219

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027600G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294432G>A , CM000673.2:g.88294432G>A	GRCh38
NC_000011.9:g.88027600G>A , CM000673.1:g.88027600G>A	GRCh37
NC_000011.8:g.87667248G>A	NCBI36
NG_007952.1:g.48342C>T , LRG_50:g.48342C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.966C>T MANE Select	ENSP00000227266.4:p.Phe322=
ENST00000533897.2:n.5279C>T
ENST00000676612.1:c.*773C>T	ENSP00000504440.1:n.*773C>T
ENST00000677208.1:c.*472C>T	ENSP00000504347.1:n.*472C>T
ENST00000677661.1:c.*643C>T	ENSP00000503323.1:n.*643C>T
ENST00000677802.1:c.*643C>T	ENSP00000504115.1:n.*643C>T
ENST00000678395.1:c.*472C>T	ENSP00000503123.1:n.*472C>T
ENST00000678464.1:c.933C>T	ENSP00000503046.1:p.Phe311=
ENST00000678506.1:c.927C>T	ENSP00000503580.1:p.Phe309=
ENST00000678520.1:c.*617C>T	ENSP00000503361.1:n.*617C>T
ENST00000678554.1:c.889+1701C>T	ENSP00000504541.1:n.889+1701C>T
ENST00000678915.1:c.834C>T	ENSP00000504805.1:p.Phe278=
ENST00000679224.1:c.603C>T	ENSP00000504475.1:p.Phe201=
ENST00000227266.9:c.966C>T	ENSP00000227266.4:p.Phe322=
ENST00000533897.1:n.3700C>T
NM_001814.4:c.966C>T , LRG_50t1:c.966C>T	NP_001805.3:p.Phe322=
NM_001814.5:c.966C>T	NP_001805.3:p.Phe322=
NM_001814.6:c.966C>T MANE Select	NP_001805.4:p.Phe322=