Canonical Allele Identifier: CA420696566

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705576T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733100T>C , CM000663.2:g.150733100T>C	GRCh38
NC_000001.10:g.150705576T>C , CM000663.1:g.150705576T>C	GRCh37
NC_000001.9:g.148972200T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.942A>G MANE Select	ENSP00000357981.3:p.Arg314=
ENST00000448301.7:c.714A>G	ENSP00000408414.2:p.Arg238=
ENST00000472977.7:c.942A>G	ENSP00000475176.2:p.Arg314=
ENST00000483930.2:c.*136A>G	ENSP00000475812.2:n.*136A>G
ENST00000607427.2:c.942A>G	ENSP00000475557.2:p.Arg314=
ENST00000679512.1:c.839A>G	ENSP00000505113.1:p.Glu280Gly
ENST00000679898.1:c.669A>G	ENSP00000505326.1:p.Arg223=
ENST00000680288.1:c.792A>G	ENSP00000506001.1:p.Arg264=
ENST00000680311.1:c.*25A>G	ENSP00000505020.1:n.*25A>G
ENST00000680471.1:c.*113A>G	ENSP00000506603.1:n.*113A>G
ENST00000680664.1:c.765A>G	ENSP00000506248.1:p.Arg255=
ENST00000680931.1:c.*292A>G	ENSP00000504934.1:n.*292A>G
ENST00000681357.1:n.332A>G
ENST00000681444.1:c.942A>G	ENSP00000505359.1:p.Arg314=
ENST00000368985.7:c.942A>G	ENSP00000357981.3:p.Arg314=
ENST00000448301.6:c.792A>G	ENSP00000408414.1:p.Arg264=
ENST00000472977.6:c.235A>G
ENST00000483930.1:c.490A>G	ENSP00000475812.1:n.490A>G
NM_001199739.1:c.792A>G	NP_001186668.1:p.Arg264=
NM_004079.4:c.942A>G	NP_004070.3:p.Arg314=
NM_004079.5:c.942A>G MANE Select	NP_004070.3:p.Arg314=
NM_001199739.2:c.792A>G	NP_001186668.1:p.Arg264=