Canonical Allele Identifier: CA342322364

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705557C>T (hg19) ; chr1:g.150733081C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733081C>T , CM000663.2:g.150733081C>T	GRCh38
NC_000001.10:g.150705557C>T , CM000663.1:g.150705557C>T	GRCh37
NC_000001.9:g.148972181C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.961G>A MANE Select	ENSP00000357981.3:p.Gly321Arg
ENST00000448301.7:c.733G>A	ENSP00000408414.2:p.Gly245Arg
ENST00000472977.7:c.961G>A	ENSP00000475176.2:p.Gly321Arg
ENST00000483930.2:c.*155G>A	ENSP00000475812.2:n.*155G>A
ENST00000607427.2:c.961G>A	ENSP00000475557.2:p.Gly321Arg
ENST00000679512.1:c.858G>A	ENSP00000505113.1:p.Val286=
ENST00000679898.1:c.688G>A	ENSP00000505326.1:p.Gly230Arg
ENST00000680288.1:c.811G>A	ENSP00000506001.1:p.Gly271Arg
ENST00000680311.1:c.*44G>A	ENSP00000505020.1:n.*44G>A
ENST00000680471.1:c.*132G>A	ENSP00000506603.1:n.*132G>A
ENST00000680664.1:c.784G>A	ENSP00000506248.1:p.Gly262Arg
ENST00000680931.1:c.*311G>A	ENSP00000504934.1:n.*311G>A
ENST00000681357.1:n.351G>A
ENST00000681444.1:c.961G>A	ENSP00000505359.1:p.Gly321Arg
ENST00000368985.7:c.961G>A	ENSP00000357981.3:p.Gly321Arg
ENST00000448301.6:c.811G>A	ENSP00000408414.1:p.Gly271Arg
ENST00000472977.6:c.254G>A
ENST00000483930.1:c.509G>A	ENSP00000475812.1:n.509G>A
NM_001199739.1:c.811G>A	NP_001186668.1:p.Gly271Arg
NM_004079.4:c.961G>A	NP_004070.3:p.Gly321Arg
NM_004079.5:c.961G>A MANE Select	NP_004070.3:p.Gly321Arg
NM_001199739.2:c.811G>A	NP_001186668.1:p.Gly271Arg