Canonical Allele Identifier: CA342322471

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705604C>A (hg19) ; chr1:g.150733128C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733128C>A , CM000663.2:g.150733128C>A	GRCh38
NC_000001.10:g.150705604C>A , CM000663.1:g.150705604C>A	GRCh37
NC_000001.9:g.148972228C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.914G>T MANE Select	ENSP00000357981.3:p.Gly305Val
ENST00000448301.7:c.686G>T	ENSP00000408414.2:p.Gly229Val
ENST00000472977.7:c.914G>T	ENSP00000475176.2:p.Gly305Val
ENST00000483930.2:c.*108G>T	ENSP00000475812.2:n.*108G>T
ENST00000607427.2:c.914G>T	ENSP00000475557.2:p.Gly305Val
ENST00000679512.1:c.811G>T	ENSP00000505113.1:p.Val271Leu
ENST00000679898.1:c.641G>T	ENSP00000505326.1:p.Gly214Val
ENST00000680288.1:c.764G>T	ENSP00000506001.1:p.Gly255Val
ENST00000680311.1:c.645G>T	ENSP00000505020.1:p.Trp215Cys
ENST00000680471.1:c.*85G>T	ENSP00000506603.1:n.*85G>T
ENST00000680664.1:c.737G>T	ENSP00000506248.1:p.Gly246Val
ENST00000680931.1:c.*264G>T	ENSP00000504934.1:n.*264G>T
ENST00000681357.1:n.304G>T
ENST00000681444.1:c.914G>T	ENSP00000505359.1:p.Gly305Val
ENST00000368985.7:c.914G>T	ENSP00000357981.3:p.Gly305Val
ENST00000448301.6:c.764G>T	ENSP00000408414.1:p.Gly255Val
ENST00000472977.6:c.207G>T
ENST00000483930.1:c.462G>T	ENSP00000475812.1:n.462G>T
NM_001199739.1:c.764G>T	NP_001186668.1:p.Gly255Val
NM_004079.4:c.914G>T	NP_004070.3:p.Gly305Val
NM_004079.5:c.914G>T MANE Select	NP_004070.3:p.Gly305Val
NM_001199739.2:c.764G>T	NP_001186668.1:p.Gly255Val