Canonical Allele Identifier: CA420696586

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705603A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733127A>G , CM000663.2:g.150733127A>G	GRCh38
NC_000001.10:g.150705603A>G , CM000663.1:g.150705603A>G	GRCh37
NC_000001.9:g.148972227A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.915T>C MANE Select	ENSP00000357981.3:p.Gly305=
ENST00000448301.7:c.687T>C	ENSP00000408414.2:p.Gly229=
ENST00000472977.7:c.915T>C	ENSP00000475176.2:p.Gly305=
ENST00000483930.2:c.*109T>C	ENSP00000475812.2:n.*109T>C
ENST00000607427.2:c.915T>C	ENSP00000475557.2:p.Gly305=
ENST00000679512.1:c.812T>C	ENSP00000505113.1:p.Val271Ala
ENST00000679898.1:c.642T>C	ENSP00000505326.1:p.Gly214=
ENST00000680288.1:c.765T>C	ENSP00000506001.1:p.Gly255=
ENST00000680311.1:c.646T>C	ENSP00000505020.1:p.Ter216Arg
ENST00000680471.1:c.*86T>C	ENSP00000506603.1:n.*86T>C
ENST00000680664.1:c.738T>C	ENSP00000506248.1:p.Gly246=
ENST00000680931.1:c.*265T>C	ENSP00000504934.1:n.*265T>C
ENST00000681357.1:n.305T>C
ENST00000681444.1:c.915T>C	ENSP00000505359.1:p.Gly305=
ENST00000368985.7:c.915T>C	ENSP00000357981.3:p.Gly305=
ENST00000448301.6:c.765T>C	ENSP00000408414.1:p.Gly255=
ENST00000472977.6:c.208T>C
ENST00000483930.1:c.463T>C	ENSP00000475812.1:n.463T>C
NM_001199739.1:c.765T>C	NP_001186668.1:p.Gly255=
NM_004079.4:c.915T>C	NP_004070.3:p.Gly305=
NM_004079.5:c.915T>C MANE Select	NP_004070.3:p.Gly305=
NM_001199739.2:c.765T>C	NP_001186668.1:p.Gly255=