Canonical Allele Identifier: CA1989489455

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88309182G= , CM000673.2:g.88309182G=	GRCh38
NC_000011.9:g.88042350G= , CM000673.1:g.88042350G=	GRCh37
NC_000011.8:g.87681998G=	NCBI36
NG_007952.1:g.33592C= , LRG_50:g.33592C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.622C= MANE Select	ENSP00000227266.4:p.His208=
ENST00000527018.6:c.622C=	ENSP00000432556.2:p.His208=
ENST00000533897.2:n.670C=
ENST00000676612.1:c.*429C=	ENSP00000504440.1:n.*429C=
ENST00000677208.1:c.*128C=	ENSP00000504347.1:n.*128C=
ENST00000677661.1:c.*299C=	ENSP00000503323.1:n.*299C=
ENST00000677802.1:c.*299C=	ENSP00000504115.1:n.*299C=
ENST00000678065.1:n.182C=
ENST00000678395.1:c.*128C=	ENSP00000503123.1:n.*128C=
ENST00000678464.1:c.622C=	ENSP00000503046.1:p.His208=
ENST00000678506.1:c.583C=	ENSP00000503580.1:p.His195=
ENST00000678520.1:c.*292+3206C=	ENSP00000503361.1:n.*292+3206C=
ENST00000678554.1:c.622C=	ENSP00000504541.1:p.His208=
ENST00000678915.1:c.622C=	ENSP00000504805.1:p.His208=
ENST00000679224.1:c.259C=	ENSP00000504475.1:p.His87=
ENST00000227266.9:c.622C=	ENSP00000227266.4:p.His208=
ENST00000527018.5:c.492C=
NM_001814.4:c.622C= , LRG_50t1:c.622C=	NP_001805.3:p.His208=
NM_001814.5:c.622C=	NP_001805.3:p.His208=
NM_001814.6:c.622C= MANE Select	NP_001805.4:p.His208=