Canonical Allele Identifier: CA1989485461

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88300515G= , CM000673.2:g.88300515G=	GRCh38
NC_000011.9:g.88033683G= , CM000673.1:g.88033683G=	GRCh37
NC_000011.8:g.87673331G=	NCBI36
NG_007952.1:g.42259C= , LRG_50:g.42259C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.757+15C= MANE Select	ENSP00000227266.4:n.757+15C=
ENST00000527018.6:c.757+15C=	ENSP00000432556.2:n.757+15C=
ENST00000533897.2:n.820C=
ENST00000676612.1:c.*564+15C=	ENSP00000504440.1:n.*564+15C=
ENST00000677208.1:c.*263+15C=	ENSP00000504347.1:n.*263+15C=
ENST00000677661.1:c.*434+15C=	ENSP00000503323.1:n.*434+15C=
ENST00000677802.1:c.*434+15C=	ENSP00000504115.1:n.*434+15C=
ENST00000678065.1:n.332C=
ENST00000678395.1:c.*263+15C=	ENSP00000503123.1:n.*263+15C=
ENST00000678464.1:c.757+15C=	ENSP00000503046.1:n.757+15C=
ENST00000678506.1:c.718+15C=	ENSP00000503580.1:n.718+15C=
ENST00000678520.1:c.*408+15C=	ENSP00000503361.1:n.*408+15C=
ENST00000678554.1:c.757+15C=	ENSP00000504541.1:n.757+15C=
ENST00000678915.1:c.757+15C=	ENSP00000504805.1:n.757+15C=
ENST00000679224.1:c.394+15C=	ENSP00000504475.1:n.394+15C=
ENST00000227266.9:c.757+15C=	ENSP00000227266.4:n.757+15C=
ENST00000527018.5:c.627+15C=
NM_001814.4:c.757+15C= , LRG_50t1:c.757+15C=	NP_001805.3:n.757+15C=
NM_001814.5:c.757+15C=	NP_001805.3:n.757+15C=
NM_001814.6:c.757+15C= MANE Select	NP_001805.4:n.757+15C=