Canonical Allele Identifier: CA1989482818

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294507G= , CM000673.2:g.88294507G=	GRCh38
NC_000011.9:g.88027675G= , CM000673.1:g.88027675G=	GRCh37
NC_000011.8:g.87667323G=	NCBI36
NG_007952.1:g.48267C= , LRG_50:g.48267C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.891C= MANE Select	ENSP00000227266.4:p.Gly297=
ENST00000533897.2:n.5204C=
ENST00000676612.1:c.*698C=	ENSP00000504440.1:n.*698C=
ENST00000677208.1:c.*397C=	ENSP00000504347.1:n.*397C=
ENST00000677661.1:c.*568C=	ENSP00000503323.1:n.*568C=
ENST00000677802.1:c.*568C=	ENSP00000504115.1:n.*568C=
ENST00000678395.1:c.*397C=	ENSP00000503123.1:n.*397C=
ENST00000678464.1:c.890-32C=	ENSP00000503046.1:n.890-32C=
ENST00000678506.1:c.852C=	ENSP00000503580.1:p.Gly284=
ENST00000678520.1:c.*542C=	ENSP00000503361.1:n.*542C=
ENST00000678554.1:c.889+1626C=	ENSP00000504541.1:n.889+1626C=
ENST00000678915.1:c.759C=	ENSP00000504805.1:p.Gly253=
ENST00000679224.1:c.528C=	ENSP00000504475.1:p.Gly176=
ENST00000227266.9:c.891C=	ENSP00000227266.4:p.Gly297=
ENST00000533897.1:n.3625C=
NM_001814.4:c.891C= , LRG_50t1:c.891C=	NP_001805.3:p.Gly297=
NM_001814.5:c.891C=	NP_001805.3:p.Gly297=
NM_001814.6:c.891C= MANE Select	NP_001805.4:p.Gly297=