Canonical Allele Identifier: CA382022138

Gene: CTSC

Linked Data

• dbSNP Id: rs1944276477
• MyVariant Identifiers: chr11:g.88027583T>A (hg19) ; chr11:g.88294415T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294415T>A , CM000673.2:g.88294415T>A	GRCh38
NC_000011.9:g.88027583T>A , CM000673.1:g.88027583T>A	GRCh37
NC_000011.8:g.87667231T>A	NCBI36
NG_007952.1:g.48359A>T , LRG_50:g.48359A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.983A>T MANE Select	ENSP00000227266.4:p.Asp328Val
ENST00000533897.2:n.5296A>T
ENST00000676612.1:c.*790A>T	ENSP00000504440.1:n.*790A>T
ENST00000677208.1:c.*489A>T	ENSP00000504347.1:n.*489A>T
ENST00000677661.1:c.*660A>T	ENSP00000503323.1:n.*660A>T
ENST00000677802.1:c.*660A>T	ENSP00000504115.1:n.*660A>T
ENST00000678395.1:c.*489A>T	ENSP00000503123.1:n.*489A>T
ENST00000678464.1:c.950A>T	ENSP00000503046.1:p.Asp317Val
ENST00000678506.1:c.944A>T	ENSP00000503580.1:p.Asp315Val
ENST00000678520.1:c.*634A>T	ENSP00000503361.1:n.*634A>T
ENST00000678554.1:c.889+1718A>T	ENSP00000504541.1:n.889+1718A>T
ENST00000678915.1:c.851A>T	ENSP00000504805.1:p.Asp284Val
ENST00000679224.1:c.620A>T	ENSP00000504475.1:p.Asp207Val
ENST00000227266.9:c.983A>T	ENSP00000227266.4:p.Asp328Val
ENST00000533897.1:n.3717A>T
NM_001814.4:c.983A>T , LRG_50t1:c.983A>T	NP_001805.3:p.Asp328Val
NM_001814.5:c.983A>T	NP_001805.3:p.Asp328Val
NM_001814.6:c.983A>T MANE Select	NP_001805.4:p.Asp328Val