Canonical Allele Identifier: CA1989482803

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294474T= , CM000673.2:g.88294474T=	GRCh38
NC_000011.9:g.88027642T= , CM000673.1:g.88027642T=	GRCh37
NC_000011.8:g.87667290T=	NCBI36
NG_007952.1:g.48300A= , LRG_50:g.48300A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.924A= MANE Select	ENSP00000227266.4:p.Gly308=
ENST00000533897.2:n.5237A=
ENST00000676612.1:c.*731A=	ENSP00000504440.1:n.*731A=
ENST00000677208.1:c.*430A=	ENSP00000504347.1:n.*430A=
ENST00000677661.1:c.*601A=	ENSP00000503323.1:n.*601A=
ENST00000677802.1:c.*601A=	ENSP00000504115.1:n.*601A=
ENST00000678395.1:c.*430A=	ENSP00000503123.1:n.*430A=
ENST00000678464.1:c.891A=	ENSP00000503046.1:p.Gly297=
ENST00000678506.1:c.885A=	ENSP00000503580.1:p.Gly295=
ENST00000678520.1:c.*575A=	ENSP00000503361.1:n.*575A=
ENST00000678554.1:c.889+1659A=	ENSP00000504541.1:n.889+1659A=
ENST00000678915.1:c.792A=	ENSP00000504805.1:p.Gly264=
ENST00000679224.1:c.561A=	ENSP00000504475.1:p.Gly187=
ENST00000227266.9:c.924A=	ENSP00000227266.4:p.Gly308=
ENST00000533897.1:n.3658A=
NM_001814.4:c.924A= , LRG_50t1:c.924A=	NP_001805.3:p.Gly308=
NM_001814.5:c.924A=	NP_001805.3:p.Gly308=
NM_001814.6:c.924A= MANE Select	NP_001805.4:p.Gly308=