Canonical Allele Identifier: CA420696569

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705579T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733103T>A , CM000663.2:g.150733103T>A	GRCh38
NC_000001.10:g.150705579T>A , CM000663.1:g.150705579T>A	GRCh37
NC_000001.9:g.148972203T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.939A>T MANE Select	ENSP00000357981.3:p.Ala313=
ENST00000448301.7:c.711A>T	ENSP00000408414.2:p.Ala237=
ENST00000472977.7:c.939A>T	ENSP00000475176.2:p.Ala313=
ENST00000483930.2:c.*133A>T	ENSP00000475812.2:n.*133A>T
ENST00000607427.2:c.939A>T	ENSP00000475557.2:p.Ala313=
ENST00000679512.1:c.836A>T	ENSP00000505113.1:p.Gln279Leu
ENST00000679898.1:c.666A>T	ENSP00000505326.1:p.Ala222=
ENST00000680288.1:c.789A>T	ENSP00000506001.1:p.Ala263=
ENST00000680311.1:c.*22A>T	ENSP00000505020.1:n.*22A>T
ENST00000680471.1:c.*110A>T	ENSP00000506603.1:n.*110A>T
ENST00000680664.1:c.762A>T	ENSP00000506248.1:p.Ala254=
ENST00000680931.1:c.*289A>T	ENSP00000504934.1:n.*289A>T
ENST00000681357.1:n.329A>T
ENST00000681444.1:c.939A>T	ENSP00000505359.1:p.Ala313=
ENST00000368985.7:c.939A>T	ENSP00000357981.3:p.Ala313=
ENST00000448301.6:c.789A>T	ENSP00000408414.1:p.Ala263=
ENST00000472977.6:c.232A>T
ENST00000483930.1:c.487A>T	ENSP00000475812.1:n.487A>T
NM_001199739.1:c.789A>T	NP_001186668.1:p.Ala263=
NM_004079.4:c.939A>T	NP_004070.3:p.Ala313=
NM_004079.5:c.939A>T MANE Select	NP_004070.3:p.Ala313=
NM_001199739.2:c.789A>T	NP_001186668.1:p.Ala263=