Canonical Allele Identifier: CA1989482796

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294462T= , CM000673.2:g.88294462T=	GRCh38
NC_000011.9:g.88027630T= , CM000673.1:g.88027630T=	GRCh37
NC_000011.8:g.87667278T=	NCBI36
NG_007952.1:g.48312A= , LRG_50:g.48312A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.936A= MANE Select	ENSP00000227266.4:p.Gln312=
ENST00000533897.2:n.5249A=
ENST00000676612.1:c.*743A=	ENSP00000504440.1:n.*743A=
ENST00000677208.1:c.*442A=	ENSP00000504347.1:n.*442A=
ENST00000677661.1:c.*613A=	ENSP00000503323.1:n.*613A=
ENST00000677802.1:c.*613A=	ENSP00000504115.1:n.*613A=
ENST00000678395.1:c.*442A=	ENSP00000503123.1:n.*442A=
ENST00000678464.1:c.903A=	ENSP00000503046.1:p.Gln301=
ENST00000678506.1:c.897A=	ENSP00000503580.1:p.Gln299=
ENST00000678520.1:c.*587A=	ENSP00000503361.1:n.*587A=
ENST00000678554.1:c.889+1671A=	ENSP00000504541.1:n.889+1671A=
ENST00000678915.1:c.804A=	ENSP00000504805.1:p.Gln268=
ENST00000679224.1:c.573A=	ENSP00000504475.1:p.Gln191=
ENST00000227266.9:c.936A=	ENSP00000227266.4:p.Gln312=
ENST00000533897.1:n.3670A=
NM_001814.4:c.936A= , LRG_50t1:c.936A=	NP_001805.3:p.Gln312=
NM_001814.5:c.936A=	NP_001805.3:p.Gln312=
NM_001814.6:c.936A= MANE Select	NP_001805.4:p.Gln312=