Canonical Allele Identifier: CA1989482756

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294356C= , CM000673.2:g.88294356C=	GRCh38
NC_000011.9:g.88027524C= , CM000673.1:g.88027524C=	GRCh37
NC_000011.8:g.87667172C=	NCBI36
NG_007952.1:g.48418G= , LRG_50:g.48418G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1042G= MANE Select	ENSP00000227266.4:p.Val348=
ENST00000533897.2:n.5355G=
ENST00000676612.1:c.*849G=	ENSP00000504440.1:n.*849G=
ENST00000677208.1:c.*548G=	ENSP00000504347.1:n.*548G=
ENST00000677661.1:c.*719G=	ENSP00000503323.1:n.*719G=
ENST00000677802.1:c.*719G=	ENSP00000504115.1:n.*719G=
ENST00000678395.1:c.*548G=	ENSP00000503123.1:n.*548G=
ENST00000678464.1:c.1009G=	ENSP00000503046.1:p.Val337=
ENST00000678506.1:c.1003G=	ENSP00000503580.1:p.Val335=
ENST00000678520.1:c.*693G=	ENSP00000503361.1:n.*693G=
ENST00000678554.1:c.889+1777G=	ENSP00000504541.1:n.889+1777G=
ENST00000678915.1:c.910G=	ENSP00000504805.1:p.Val304=
ENST00000679224.1:c.679G=	ENSP00000504475.1:p.Val227=
ENST00000227266.9:c.1042G=	ENSP00000227266.4:p.Val348=
ENST00000533897.1:n.3776G=
NM_001814.4:c.1042G= , LRG_50t1:c.1042G=	NP_001805.3:p.Val348=
NM_001814.5:c.1042G=	NP_001805.3:p.Val348=
NM_001814.6:c.1042G= MANE Select	NP_001805.4:p.Val348=