Canonical Allele Identifier: CA476145237

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027633G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294465G>T , CM000673.2:g.88294465G>T	GRCh38
NC_000011.9:g.88027633G>T , CM000673.1:g.88027633G>T	GRCh37
NC_000011.8:g.87667281G>T	NCBI36
NG_007952.1:g.48309C>A , LRG_50:g.48309C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.933C>A MANE Select	ENSP00000227266.4:p.Ala311=
ENST00000533897.2:n.5246C>A
ENST00000676612.1:c.*740C>A	ENSP00000504440.1:n.*740C>A
ENST00000677208.1:c.*439C>A	ENSP00000504347.1:n.*439C>A
ENST00000677661.1:c.*610C>A	ENSP00000503323.1:n.*610C>A
ENST00000677802.1:c.*610C>A	ENSP00000504115.1:n.*610C>A
ENST00000678395.1:c.*439C>A	ENSP00000503123.1:n.*439C>A
ENST00000678464.1:c.900C>A	ENSP00000503046.1:p.Ala300=
ENST00000678506.1:c.894C>A	ENSP00000503580.1:p.Ala298=
ENST00000678520.1:c.*584C>A	ENSP00000503361.1:n.*584C>A
ENST00000678554.1:c.889+1668C>A	ENSP00000504541.1:n.889+1668C>A
ENST00000678915.1:c.801C>A	ENSP00000504805.1:p.Ala267=
ENST00000679224.1:c.570C>A	ENSP00000504475.1:p.Ala190=
ENST00000227266.9:c.933C>A	ENSP00000227266.4:p.Ala311=
ENST00000533897.1:n.3667C>A
NM_001814.4:c.933C>A , LRG_50t1:c.933C>A	NP_001805.3:p.Ala311=
NM_001814.5:c.933C>A	NP_001805.3:p.Ala311=
NM_001814.6:c.933C>A MANE Select	NP_001805.4:p.Ala311=