Canonical Allele Identifier: CA382022277

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027644C>T (hg19) ; chr11:g.88294476C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294476C>T , CM000673.2:g.88294476C>T	GRCh38
NC_000011.9:g.88027644C>T , CM000673.1:g.88027644C>T	GRCh37
NC_000011.8:g.87667292C>T	NCBI36
NG_007952.1:g.48298G>A , LRG_50:g.48298G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.922G>A MANE Select	ENSP00000227266.4:p.Gly308Arg
ENST00000533897.2:n.5235G>A
ENST00000676612.1:c.*729G>A	ENSP00000504440.1:n.*729G>A
ENST00000677208.1:c.*428G>A	ENSP00000504347.1:n.*428G>A
ENST00000677661.1:c.*599G>A	ENSP00000503323.1:n.*599G>A
ENST00000677802.1:c.*599G>A	ENSP00000504115.1:n.*599G>A
ENST00000678395.1:c.*428G>A	ENSP00000503123.1:n.*428G>A
ENST00000678464.1:c.890-1G>A	ENSP00000503046.1:n.890-1G>A
ENST00000678506.1:c.883G>A	ENSP00000503580.1:p.Gly295Arg
ENST00000678520.1:c.*573G>A	ENSP00000503361.1:n.*573G>A
ENST00000678554.1:c.889+1657G>A	ENSP00000504541.1:n.889+1657G>A
ENST00000678915.1:c.790G>A	ENSP00000504805.1:p.Gly264Arg
ENST00000679224.1:c.559G>A	ENSP00000504475.1:p.Gly187Arg
ENST00000227266.9:c.922G>A	ENSP00000227266.4:p.Gly308Arg
ENST00000533897.1:n.3656G>A
NM_001814.4:c.922G>A , LRG_50t1:c.922G>A	NP_001805.3:p.Gly308Arg
NM_001814.5:c.922G>A	NP_001805.3:p.Gly308Arg
NM_001814.6:c.922G>A MANE Select	NP_001805.4:p.Gly308Arg