Canonical Allele Identifier: CA1989482752

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294350C= , CM000673.2:g.88294350C=	GRCh38
NC_000011.9:g.88027518C= , CM000673.1:g.88027518C=	GRCh37
NC_000011.8:g.87667166C=	NCBI36
NG_007952.1:g.48424G= , LRG_50:g.48424G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1048G= MANE Select	ENSP00000227266.4:p.Gly350=
ENST00000533897.2:n.5361G=
ENST00000676612.1:c.*855G=	ENSP00000504440.1:n.*855G=
ENST00000677208.1:c.*554G=	ENSP00000504347.1:n.*554G=
ENST00000677661.1:c.*725G=	ENSP00000503323.1:n.*725G=
ENST00000677802.1:c.*725G=	ENSP00000504115.1:n.*725G=
ENST00000678395.1:c.*554G=	ENSP00000503123.1:n.*554G=
ENST00000678464.1:c.1015G=	ENSP00000503046.1:p.Gly339=
ENST00000678506.1:c.1009G=	ENSP00000503580.1:p.Gly337=
ENST00000678520.1:c.*699G=	ENSP00000503361.1:n.*699G=
ENST00000678554.1:c.889+1783G=	ENSP00000504541.1:n.889+1783G=
ENST00000678915.1:c.916G=	ENSP00000504805.1:p.Gly306=
ENST00000679224.1:c.685G=	ENSP00000504475.1:p.Gly229=
ENST00000227266.9:c.1048G=	ENSP00000227266.4:p.Gly350=
ENST00000533897.1:n.3782G=
NM_001814.4:c.1048G= , LRG_50t1:c.1048G=	NP_001805.3:p.Gly350=
NM_001814.5:c.1048G=	NP_001805.3:p.Gly350=
NM_001814.6:c.1048G= MANE Select	NP_001805.4:p.Gly350=