Canonical Allele Identifier: CA476145398

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027519T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294351T>G , CM000673.2:g.88294351T>G	GRCh38
NC_000011.9:g.88027519T>G , CM000673.1:g.88027519T>G	GRCh37
NC_000011.8:g.87667167T>G	NCBI36
NG_007952.1:g.48423A>C , LRG_50:g.48423A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1047A>C MANE Select	ENSP00000227266.4:p.Gly349=
ENST00000533897.2:n.5360A>C
ENST00000676612.1:c.*854A>C	ENSP00000504440.1:n.*854A>C
ENST00000677208.1:c.*553A>C	ENSP00000504347.1:n.*553A>C
ENST00000677661.1:c.*724A>C	ENSP00000503323.1:n.*724A>C
ENST00000677802.1:c.*724A>C	ENSP00000504115.1:n.*724A>C
ENST00000678395.1:c.*553A>C	ENSP00000503123.1:n.*553A>C
ENST00000678464.1:c.1014A>C	ENSP00000503046.1:p.Gly338=
ENST00000678506.1:c.1008A>C	ENSP00000503580.1:p.Gly336=
ENST00000678520.1:c.*698A>C	ENSP00000503361.1:n.*698A>C
ENST00000678554.1:c.889+1782A>C	ENSP00000504541.1:n.889+1782A>C
ENST00000678915.1:c.915A>C	ENSP00000504805.1:p.Gly305=
ENST00000679224.1:c.684A>C	ENSP00000504475.1:p.Gly228=
ENST00000227266.9:c.1047A>C	ENSP00000227266.4:p.Gly349=
ENST00000533897.1:n.3781A>C
NM_001814.4:c.1047A>C , LRG_50t1:c.1047A>C	NP_001805.3:p.Gly349=
NM_001814.5:c.1047A>C	NP_001805.3:p.Gly349=
NM_001814.6:c.1047A>C MANE Select	NP_001805.4:p.Gly349=