Canonical Allele Identifier: CA1989482735

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294312A= , CM000673.2:g.88294312A=	GRCh38
NC_000011.9:g.88027480A= , CM000673.1:g.88027480A=	GRCh37
NC_000011.8:g.87667128A=	NCBI36
NG_007952.1:g.48462T= , LRG_50:g.48462T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.1086T= MANE Select	ENSP00000227266.4:p.Leu362=
ENST00000533897.2:n.5399T=
ENST00000676612.1:c.*893T=	ENSP00000504440.1:n.*893T=
ENST00000677208.1:c.*592T=	ENSP00000504347.1:n.*592T=
ENST00000677661.1:c.*763T=	ENSP00000503323.1:n.*763T=
ENST00000677802.1:c.*763T=	ENSP00000504115.1:n.*763T=
ENST00000678395.1:c.*592T=	ENSP00000503123.1:n.*592T=
ENST00000678464.1:c.1053T=	ENSP00000503046.1:p.Leu351=
ENST00000678506.1:c.1047T=	ENSP00000503580.1:p.Leu349=
ENST00000678520.1:c.*737T=	ENSP00000503361.1:n.*737T=
ENST00000678554.1:c.889+1821T=	ENSP00000504541.1:n.889+1821T=
ENST00000678915.1:c.954T=	ENSP00000504805.1:p.Leu318=
ENST00000679224.1:c.723T=	ENSP00000504475.1:p.Leu241=
ENST00000227266.9:c.1086T=	ENSP00000227266.4:p.Leu362=
ENST00000533897.1:n.3820T=
NM_001814.4:c.1086T= , LRG_50t1:c.1086T=	NP_001805.3:p.Leu362=
NM_001814.5:c.1086T=	NP_001805.3:p.Leu362=
NM_001814.6:c.1086T= MANE Select	NP_001805.4:p.Leu362=