Canonical Allele Identifier: CA1989490937
Gene: CTSC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88312401T= , CM000673.2:g.88312401T= GRCh38
NC_000011.9:g.88045569T= , CM000673.1:g.88045569T= GRCh37
NC_000011.8:g.87685217T= NCBI36
NG_007952.1:g.30373A= , LRG_50:g.30373A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227266.10:c.472A= MANE Select ENSP00000227266.4:p.Asn158=
ENST00000527018.6:c.472A= ENSP00000432556.2:p.Asn158=
ENST00000533897.2:n.520A=
ENST00000676612.1:c.*279A= ENSP00000504440.1:n.*279A=
ENST00000677208.1:c.319-3083A= ENSP00000504347.1:n.319-3083A=
ENST00000677661.1:c.*149A= ENSP00000503323.1:n.*149A=
ENST00000677802.1:c.*149A= ENSP00000504115.1:n.*149A=
ENST00000678395.1:c.423+49A= ENSP00000503123.1:n.423+49A=
ENST00000678464.1:c.472A= ENSP00000503046.1:p.Asn158=
ENST00000678506.1:c.446+26A= ENSP00000503580.1:n.446+26A=
ENST00000678520.1:c.*279A= ENSP00000503361.1:n.*279A=
ENST00000678554.1:c.472A= ENSP00000504541.1:p.Asn158=
ENST00000678915.1:c.472A= ENSP00000504805.1:p.Asn158=
ENST00000679224.1:c.109A= ENSP00000504475.1:p.Asn37=
ENST00000227266.9:c.472A= ENSP00000227266.4:p.Asn158=
ENST00000527018.5:c.342A=
ENST00000533865.5:n.494A=
NM_001814.4:c.472A= , LRG_50t1:c.472A= NP_001805.3:p.Asn158=
NM_001814.5:c.472A= NP_001805.3:p.Asn158=
NM_001814.6:c.472A= MANE Select NP_001805.4:p.Asn158=