Canonical Allele Identifier: CA342336695

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804190-C-G
• MyVariant Identifiers: chr1:g.150776666C>G (hg19) ; chr1:g.150804190C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804190C>G , CM000663.2:g.150804190C>G	GRCh38
NC_000001.10:g.150776666C>G , CM000663.1:g.150776666C>G	GRCh37
NC_000001.9:g.149043290C>G	NCBI36
NG_011848.1:g.9147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.449G>C MANE Select	ENSP00000271651.3:p.Gly150Ala
ENST00000443913.2:c.626G>C	ENSP00000405083.2:p.Gly209Ala
ENST00000480670.2:n.3518G>C
ENST00000676680.1:c.449G>C	ENSP00000503270.1:p.Gly150Ala
ENST00000676716.1:c.326G>C	ENSP00000504737.1:p.Gly109Ala
ENST00000676751.1:c.449G>C	ENSP00000502964.1:p.Gly150Ala
ENST00000676824.1:c.449G>C	ENSP00000504176.1:p.Gly150Ala
ENST00000676966.1:c.449G>C	ENSP00000503723.1:p.Gly150Ala
ENST00000676970.1:c.449G>C	ENSP00000503832.1:p.Gly150Ala
ENST00000677330.1:n.2275G>C
ENST00000677611.1:n.301G>C
ENST00000677887.1:c.491G>C	ENSP00000503876.1:p.Gly164Ala
ENST00000678275.1:c.*341G>C	ENSP00000504796.1:n.*341G>C
ENST00000678337.1:c.485G>C	ENSP00000504759.1:p.Gly162Ala
ENST00000678725.1:n.1426G>C
ENST00000679090.1:n.1034G>C
ENST00000679148.1:n.3411G>C
ENST00000679171.1:n.2810G>C
ENST00000679260.1:c.399+1671G>C	ENSP00000504534.1:n.399+1671G>C
ENST00000271651.7:c.449G>C	ENSP00000271651.3:p.Gly150Ala
ENST00000443913.1:c.626G>C	ENSP00000405083.1:p.Gly209Ala
ENST00000480670.1:n.289G>C
NM_000396.3:c.449G>C	NP_000387.1:p.Gly150Ala
NM_000396.4:c.449G>C MANE Select	NP_000387.1:p.Gly150Ala