Canonical Allele Identifier: CA2581039351

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294342A= , CM000673.2:g.88294342A=	GRCh38
NC_000011.9:g.88027510A= , CM000673.1:g.88027510A=	GRCh37
NC_000011.8:g.87667158A=	NCBI36
NG_007952.1:g.48432T= , LRG_50:g.48432T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001814.6:c.1056T= MANE Select	NP_001805.4:p.Tyr352=
ENST00000227266.10:c.1056T= MANE Select	ENSP00000227266.4:p.Tyr352=
NM_001814.4:c.1056T= , LRG_50t1:c.1056T=	NP_001805.3:p.Tyr352=
NM_001814.5:c.1056T=	NP_001805.3:p.Tyr352=
ENST00000227266.9:c.1056T=	ENSP00000227266.4:p.Tyr352=
ENST00000533897.1:n.3790T=
ENST00000533897.2:n.5369T=
ENST00000676612.1:c.*863T=	ENSP00000504440.1:n.*863T=
ENST00000677208.1:c.*562T=	ENSP00000504347.1:n.*562T=
ENST00000677661.1:c.*733T=	ENSP00000503323.1:n.*733T=
ENST00000677802.1:c.*733T=	ENSP00000504115.1:n.*733T=
ENST00000678395.1:c.*562T=	ENSP00000503123.1:n.*562T=
ENST00000678464.1:c.1023T=	ENSP00000503046.1:p.Tyr341=
ENST00000678506.1:c.1017T=	ENSP00000503580.1:p.Tyr339=
ENST00000678520.1:c.*707T=	ENSP00000503361.1:n.*707T=
ENST00000678554.1:c.889+1791T=	ENSP00000504541.1:n.889+1791T=
ENST00000678915.1:c.924T=	ENSP00000504805.1:p.Tyr308=
ENST00000679224.1:c.693T=	ENSP00000504475.1:p.Tyr231=