Canonical Allele Identifier: CA420697850

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150722597C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150750121C>T , CM000663.2:g.150750121C>T	GRCh38
NC_000001.10:g.150722597C>T , CM000663.1:g.150722597C>T	GRCh37
NC_000001.9:g.148989221C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.678G>A MANE Select	ENSP00000357981.3:p.Lys226=
ENST00000448301.7:c.450G>A	ENSP00000408414.2:p.Lys150=
ENST00000472977.7:c.678G>A	ENSP00000475176.2:p.Lys226=
ENST00000483930.2:c.678G>A	ENSP00000475812.2:p.Lys226=
ENST00000607427.2:c.678G>A	ENSP00000475557.2:p.Lys226=
ENST00000679512.1:c.678G>A	ENSP00000505113.1:p.Lys226=
ENST00000679898.1:c.405G>A	ENSP00000505326.1:p.Lys135=
ENST00000680288.1:c.528G>A	ENSP00000506001.1:p.Lys176=
ENST00000680311.1:c.627+1660G>A	ENSP00000505020.1:n.627+1660G>A
ENST00000680471.1:c.627+1660G>A	ENSP00000506603.1:n.627+1660G>A
ENST00000680664.1:c.501G>A	ENSP00000506248.1:p.Lys167=
ENST00000680931.1:c.678G>A	ENSP00000504934.1:p.Lys226=
ENST00000681444.1:c.678G>A	ENSP00000505359.1:p.Lys226=
ENST00000681728.1:c.678G>A	ENSP00000505313.1:p.Lys226=
ENST00000368985.7:c.678G>A	ENSP00000357981.3:p.Lys226=
ENST00000448301.6:c.528G>A	ENSP00000408414.1:p.Lys176=
ENST00000480760.1:n.566+1660G>A
ENST00000483930.1:c.105G>A	ENSP00000475812.1:p.Lys35=
NM_001199739.1:c.528G>A	NP_001186668.1:p.Lys176=
NM_004079.4:c.678G>A	NP_004070.3:p.Lys226=
NM_004079.5:c.678G>A MANE Select	NP_004070.3:p.Lys226=
NM_001199739.2:c.528G>A	NP_001186668.1:p.Lys176=