Canonical Allele Identifier: CA382022151

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027589C>G (hg19) ; chr11:g.88294421C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294421C>G , CM000673.2:g.88294421C>G	GRCh38
NC_000011.9:g.88027589C>G , CM000673.1:g.88027589C>G	GRCh37
NC_000011.8:g.87667237C>G	NCBI36
NG_007952.1:g.48353G>C , LRG_50:g.48353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.977G>C MANE Select	ENSP00000227266.4:p.Gly326Ala
ENST00000533897.2:n.5290G>C
ENST00000676612.1:c.*784G>C	ENSP00000504440.1:n.*784G>C
ENST00000677208.1:c.*483G>C	ENSP00000504347.1:n.*483G>C
ENST00000677661.1:c.*654G>C	ENSP00000503323.1:n.*654G>C
ENST00000677802.1:c.*654G>C	ENSP00000504115.1:n.*654G>C
ENST00000678395.1:c.*483G>C	ENSP00000503123.1:n.*483G>C
ENST00000678464.1:c.944G>C	ENSP00000503046.1:p.Gly315Ala
ENST00000678506.1:c.938G>C	ENSP00000503580.1:p.Gly313Ala
ENST00000678520.1:c.*628G>C	ENSP00000503361.1:n.*628G>C
ENST00000678554.1:c.889+1712G>C	ENSP00000504541.1:n.889+1712G>C
ENST00000678915.1:c.845G>C	ENSP00000504805.1:p.Gly282Ala
ENST00000679224.1:c.614G>C	ENSP00000504475.1:p.Gly205Ala
ENST00000227266.9:c.977G>C	ENSP00000227266.4:p.Gly326Ala
ENST00000533897.1:n.3711G>C
NM_001814.4:c.977G>C , LRG_50t1:c.977G>C	NP_001805.3:p.Gly326Ala
NM_001814.5:c.977G>C	NP_001805.3:p.Gly326Ala
NM_001814.6:c.977G>C MANE Select	NP_001805.4:p.Gly326Ala