Canonical Allele Identifier: CA342322415

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705578T>A (hg19) ; chr1:g.150733102T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733102T>A , CM000663.2:g.150733102T>A	GRCh38
NC_000001.10:g.150705578T>A , CM000663.1:g.150705578T>A	GRCh37
NC_000001.9:g.148972202T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.940A>T MANE Select	ENSP00000357981.3:p.Arg314Ter
ENST00000448301.7:c.712A>T	ENSP00000408414.2:p.Arg238Ter
ENST00000472977.7:c.940A>T	ENSP00000475176.2:p.Arg314Ter
ENST00000483930.2:c.*134A>T	ENSP00000475812.2:n.*134A>T
ENST00000607427.2:c.940A>T	ENSP00000475557.2:p.Arg314Ter
ENST00000679512.1:c.837A>T	ENSP00000505113.1:p.Gln279His
ENST00000679898.1:c.667A>T	ENSP00000505326.1:p.Arg223Ter
ENST00000680288.1:c.790A>T	ENSP00000506001.1:p.Arg264Ter
ENST00000680311.1:c.*23A>T	ENSP00000505020.1:n.*23A>T
ENST00000680471.1:c.*111A>T	ENSP00000506603.1:n.*111A>T
ENST00000680664.1:c.763A>T	ENSP00000506248.1:p.Arg255Ter
ENST00000680931.1:c.*290A>T	ENSP00000504934.1:n.*290A>T
ENST00000681357.1:n.330A>T
ENST00000681444.1:c.940A>T	ENSP00000505359.1:p.Arg314Ter
ENST00000368985.7:c.940A>T	ENSP00000357981.3:p.Arg314Ter
ENST00000448301.6:c.790A>T	ENSP00000408414.1:p.Arg264Ter
ENST00000472977.6:c.233A>T
ENST00000483930.1:c.488A>T	ENSP00000475812.1:n.488A>T
NM_001199739.1:c.790A>T	NP_001186668.1:p.Arg264Ter
NM_004079.4:c.940A>T	NP_004070.3:p.Arg314Ter
NM_004079.5:c.940A>T MANE Select	NP_004070.3:p.Arg314Ter
NM_001199739.2:c.790A>T	NP_001186668.1:p.Arg264Ter