Canonical Allele Identifier: CA342336349

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776510G>C (hg19) ; chr1:g.150804034G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804034G>C , CM000663.2:g.150804034G>C	GRCh38
NC_000001.10:g.150776510G>C , CM000663.1:g.150776510G>C	GRCh37
NC_000001.9:g.149043134G>C	NCBI36
NG_011848.1:g.9303C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.605C>G MANE Select	ENSP00000271651.3:p.Pro202Arg
ENST00000443913.2:c.782C>G	ENSP00000405083.2:p.Pro261Arg
ENST00000480670.2:n.3674C>G
ENST00000676680.1:c.605C>G	ENSP00000503270.1:p.Pro202Arg
ENST00000676716.1:c.482C>G	ENSP00000504737.1:p.Pro161Arg
ENST00000676751.1:c.605C>G	ENSP00000502964.1:p.Pro202Arg
ENST00000676824.1:c.605C>G	ENSP00000504176.1:p.Pro202Arg
ENST00000676966.1:c.605C>G	ENSP00000503723.1:p.Pro202Arg
ENST00000676970.1:c.605C>G	ENSP00000503832.1:p.Pro202Arg
ENST00000677330.1:n.2431C>G
ENST00000677611.1:n.457C>G
ENST00000677887.1:c.647C>G	ENSP00000503876.1:p.Pro216Arg
ENST00000678275.1:c.*497C>G	ENSP00000504796.1:n.*497C>G
ENST00000678337.1:c.641C>G	ENSP00000504759.1:p.Pro214Arg
ENST00000678725.1:n.1582C>G
ENST00000679090.1:n.1190C>G
ENST00000679148.1:n.3567C>G
ENST00000679171.1:n.2966C>G
ENST00000679260.1:c.399+1827C>G	ENSP00000504534.1:n.399+1827C>G
ENST00000271651.7:c.605C>G	ENSP00000271651.3:p.Pro202Arg
ENST00000480670.1:n.445C>G
NM_000396.3:c.605C>G	NP_000387.1:p.Pro202Arg
NM_000396.4:c.605C>G MANE Select	NP_000387.1:p.Pro202Arg