Canonical Allele Identifier: CA658821134
Gene: CTSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150796898_150796920dup , CM000663.2:g.150796898_150796920dup GRCh38
NC_000001.10:g.150769374_150769396dup , CM000663.1:g.150769374_150769396dup GRCh37
NC_000001.9:g.149035998_149036020dup NCBI36
NG_011848.1:g.16418_16440dup

Transcript Alleles

HGVS Amino-acid Change
NM_000396.3:c.891-21_892dup
NM_000396.4:c.891-21_892dup
ENST00000271651.7:c.891-21_892dup
ENST00000271651.8:c.891-21_892dup
ENST00000443913.2:c.1068-21_1069dup
ENST00000480670.2:n.3960-21_3961dup
ENST00000676680.1:c.*185-21_*186dup
ENST00000676716.1:c.768-21_769dup
ENST00000676751.1:c.785-21_786dup
ENST00000676824.1:c.891-21_892dup
ENST00000676966.1:c.891-21_892dup
ENST00000676970.1:c.903-21_904dup
ENST00000677330.1:n.2717-21_2718dup
ENST00000677611.1:n.743-21_744dup
ENST00000677887.1:c.933-21_934dup
ENST00000678275.1:c.*783-21_*784dup
ENST00000678337.1:c.927-21_928dup
ENST00000678725.1:n.2138-21_2139dup
ENST00000679090.1:n.1746-21_1747dup
ENST00000679148.1:n.3853-21_3854dup
ENST00000679171.1:n.3522-21_3523dup
ENST00000679178.1:n.602-21_603dup
ENST00000679260.1:c.672-21_673dup