Canonical Allele Identifier: CA2479315176

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806686_150806689delinsCTTG , CM000663.2:g.150806686_150806689delinsCTTG	GRCh38
NC_000001.10:g.150779162_150779165delinsCTTG , CM000663.1:g.150779162_150779165delinsCTTG	GRCh37
NC_000001.9:g.149045786_149045789delinsCTTG	NCBI36
NG_011848.1:g.6648_6651delinsCAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.117_120delinsCAAG MANE Select	ENSP00000271651.3:p.Asn39=
ENST00000443913.2:c.294_297delinsCAAG	ENSP00000405083.2:p.Asn98=
ENST00000480670.2:n.2725_2728delinsCAAG
ENST00000676680.1:c.117_120delinsCAAG	ENSP00000503270.1:p.Asn39=
ENST00000676716.1:c.117_120delinsCAAG	ENSP00000504737.1:p.Asn39=
ENST00000676751.1:c.117_120delinsCAAG	ENSP00000502964.1:p.Asn39=
ENST00000676824.1:c.117_120delinsCAAG	ENSP00000504176.1:p.Asn39=
ENST00000676966.1:c.117_120delinsCAAG	ENSP00000503723.1:p.Asn39=
ENST00000676970.1:c.117_120delinsCAAG	ENSP00000503832.1:p.Asn39=
ENST00000677330.1:n.1482_1485delinsCAAG
ENST00000677887.1:c.159_162delinsCAAG	ENSP00000503876.1:p.Asn53=
ENST00000678275.1:c.117_120delinsCAAG	ENSP00000504796.1:p.Asn39=
ENST00000678337.1:c.153_156delinsCAAG	ENSP00000504759.1:p.Asn51=
ENST00000678725.1:n.1094_1097delinsCAAG
ENST00000679090.1:n.241_244delinsCAAG
ENST00000679148.1:n.997_1000delinsCAAG
ENST00000679171.1:n.2017_2020delinsCAAG
ENST00000679260.1:c.117_120delinsCAAG	ENSP00000504534.1:p.Asn39=
ENST00000271651.7:c.117_120delinsCAAG	ENSP00000271651.3:p.Asn39=
ENST00000443913.1:c.294_297delinsCAAG	ENSP00000405083.1:p.Asn98=
ENST00000480670.1:n.80_83delinsCAAG
NM_000396.3:c.117_120delinsCAAG	NP_000387.1:p.Asn39=
NM_000396.4:c.117_120delinsCAAG MANE Select	NP_000387.1:p.Asn39=