Canonical Allele Identifier: CA342336463

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776561G>T (hg19) ; chr1:g.150804085G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804085G>T , CM000663.2:g.150804085G>T	GRCh38
NC_000001.10:g.150776561G>T , CM000663.1:g.150776561G>T	GRCh37
NC_000001.9:g.149043185G>T	NCBI36
NG_011848.1:g.9252C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.554C>A MANE Select	ENSP00000271651.3:p.Ala185Asp
ENST00000443913.2:c.731C>A	ENSP00000405083.2:p.Ala244Asp
ENST00000480670.2:n.3623C>A
ENST00000676680.1:c.554C>A	ENSP00000503270.1:p.Ala185Asp
ENST00000676716.1:c.431C>A	ENSP00000504737.1:p.Ala144Asp
ENST00000676751.1:c.554C>A	ENSP00000502964.1:p.Ala185Asp
ENST00000676824.1:c.554C>A	ENSP00000504176.1:p.Ala185Asp
ENST00000676966.1:c.554C>A	ENSP00000503723.1:p.Ala185Asp
ENST00000676970.1:c.554C>A	ENSP00000503832.1:p.Ala185Asp
ENST00000677330.1:n.2380C>A
ENST00000677611.1:n.406C>A
ENST00000677887.1:c.596C>A	ENSP00000503876.1:p.Ala199Asp
ENST00000678275.1:c.*446C>A	ENSP00000504796.1:n.*446C>A
ENST00000678337.1:c.590C>A	ENSP00000504759.1:p.Ala197Asp
ENST00000678725.1:n.1531C>A
ENST00000679090.1:n.1139C>A
ENST00000679148.1:n.3516C>A
ENST00000679171.1:n.2915C>A
ENST00000679260.1:c.399+1776C>A	ENSP00000504534.1:n.399+1776C>A
ENST00000271651.7:c.554C>A	ENSP00000271651.3:p.Ala185Asp
ENST00000443913.1:c.731C>A	ENSP00000405083.1:p.Ala244Asp
ENST00000480670.1:n.394C>A
NM_000396.3:c.554C>A	NP_000387.1:p.Ala185Asp
NM_000396.4:c.554C>A MANE Select	NP_000387.1:p.Ala185Asp