Canonical Allele Identifier: CA382024959

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88042355C>A (hg19) ; chr11:g.88309187C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88309187C>A , CM000673.2:g.88309187C>A	GRCh38
NC_000011.9:g.88042355C>A , CM000673.1:g.88042355C>A	GRCh37
NC_000011.8:g.87682003C>A	NCBI36
NG_007952.1:g.33587G>T , LRG_50:g.33587G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.617G>T MANE Select	ENSP00000227266.4:p.Gly206Val
ENST00000527018.6:c.617G>T	ENSP00000432556.2:p.Gly206Val
ENST00000533897.2:n.665G>T
ENST00000676612.1:c.*424G>T	ENSP00000504440.1:n.*424G>T
ENST00000677208.1:c.*123G>T	ENSP00000504347.1:n.*123G>T
ENST00000677661.1:c.*294G>T	ENSP00000503323.1:n.*294G>T
ENST00000677802.1:c.*294G>T	ENSP00000504115.1:n.*294G>T
ENST00000678065.1:n.177G>T
ENST00000678395.1:c.*123G>T	ENSP00000503123.1:n.*123G>T
ENST00000678464.1:c.617G>T	ENSP00000503046.1:p.Gly206Val
ENST00000678506.1:c.578G>T	ENSP00000503580.1:p.Gly193Val
ENST00000678520.1:c.*292+3201G>T	ENSP00000503361.1:n.*292+3201G>T
ENST00000678554.1:c.617G>T	ENSP00000504541.1:p.Gly206Val
ENST00000678915.1:c.617G>T	ENSP00000504805.1:p.Gly206Val
ENST00000679224.1:c.254G>T	ENSP00000504475.1:p.Gly85Val
ENST00000227266.9:c.617G>T	ENSP00000227266.4:p.Gly206Val
ENST00000527018.5:c.487G>T
NM_001814.4:c.617G>T , LRG_50t1:c.617G>T	NP_001805.3:p.Gly206Val
NM_001814.5:c.617G>T	NP_001805.3:p.Gly206Val
NM_001814.6:c.617G>T MANE Select	NP_001805.4:p.Gly206Val