Canonical Allele Identifier: CA342322476

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705605C>T (hg19) ; chr1:g.150733129C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733129C>T , CM000663.2:g.150733129C>T	GRCh38
NC_000001.10:g.150705605C>T , CM000663.1:g.150705605C>T	GRCh37
NC_000001.9:g.148972229C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.913G>A MANE Select	ENSP00000357981.3:p.Gly305Ser
ENST00000448301.7:c.685G>A	ENSP00000408414.2:p.Gly229Ser
ENST00000472977.7:c.913G>A	ENSP00000475176.2:p.Gly305Ser
ENST00000483930.2:c.*107G>A	ENSP00000475812.2:n.*107G>A
ENST00000607427.2:c.913G>A	ENSP00000475557.2:p.Gly305Ser
ENST00000679512.1:c.810G>A	ENSP00000505113.1:p.Leu270=
ENST00000679898.1:c.640G>A	ENSP00000505326.1:p.Gly214Ser
ENST00000680288.1:c.763G>A	ENSP00000506001.1:p.Gly255Ser
ENST00000680311.1:c.644G>A	ENSP00000505020.1:p.Trp215Ter
ENST00000680471.1:c.*84G>A	ENSP00000506603.1:n.*84G>A
ENST00000680664.1:c.736G>A	ENSP00000506248.1:p.Gly246Ser
ENST00000680931.1:c.*263G>A	ENSP00000504934.1:n.*263G>A
ENST00000681357.1:n.303G>A
ENST00000681444.1:c.913G>A	ENSP00000505359.1:p.Gly305Ser
ENST00000368985.7:c.913G>A	ENSP00000357981.3:p.Gly305Ser
ENST00000448301.6:c.763G>A	ENSP00000408414.1:p.Gly255Ser
ENST00000472977.6:c.206G>A
ENST00000483930.1:c.461G>A	ENSP00000475812.1:n.461G>A
NM_001199739.1:c.763G>A	NP_001186668.1:p.Gly255Ser
NM_004079.4:c.913G>A	NP_004070.3:p.Gly305Ser
NM_004079.5:c.913G>A MANE Select	NP_004070.3:p.Gly305Ser
NM_001199739.2:c.763G>A	NP_001186668.1:p.Gly255Ser