Canonical Allele Identifier: CA342322465

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705601T>A (hg19) ; chr1:g.150733125T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733125T>A , CM000663.2:g.150733125T>A	GRCh38
NC_000001.10:g.150705601T>A , CM000663.1:g.150705601T>A	GRCh37
NC_000001.9:g.148972225T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.917A>T MANE Select	ENSP00000357981.3:p.Glu306Val
ENST00000448301.7:c.689A>T	ENSP00000408414.2:p.Glu230Val
ENST00000472977.7:c.917A>T	ENSP00000475176.2:p.Glu306Val
ENST00000483930.2:c.*111A>T	ENSP00000475812.2:n.*111A>T
ENST00000607427.2:c.917A>T	ENSP00000475557.2:p.Glu306Val
ENST00000679512.1:c.814A>T	ENSP00000505113.1:p.Lys272Ter
ENST00000679898.1:c.644A>T	ENSP00000505326.1:p.Glu215Val
ENST00000680288.1:c.767A>T	ENSP00000506001.1:p.Glu256Val
ENST00000680311.1:c.648A>T	ENSP00000505020.1:p.Ter216Cys
ENST00000680471.1:c.*88A>T	ENSP00000506603.1:n.*88A>T
ENST00000680664.1:c.740A>T	ENSP00000506248.1:p.Glu247Val
ENST00000680931.1:c.*267A>T	ENSP00000504934.1:n.*267A>T
ENST00000681357.1:n.307A>T
ENST00000681444.1:c.917A>T	ENSP00000505359.1:p.Glu306Val
ENST00000368985.7:c.917A>T	ENSP00000357981.3:p.Glu306Val
ENST00000448301.6:c.767A>T	ENSP00000408414.1:p.Glu256Val
ENST00000472977.6:c.210A>T
ENST00000483930.1:c.465A>T	ENSP00000475812.1:n.465A>T
NM_001199739.1:c.767A>T	NP_001186668.1:p.Glu256Val
NM_004079.4:c.917A>T	NP_004070.3:p.Glu306Val
NM_004079.5:c.917A>T MANE Select	NP_004070.3:p.Glu306Val
NM_001199739.2:c.767A>T	NP_001186668.1:p.Glu256Val