Canonical Allele Identifier: CA342322444

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705592T>G (hg19) ; chr1:g.150733116T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733116T>G , CM000663.2:g.150733116T>G	GRCh38
NC_000001.10:g.150705592T>G , CM000663.1:g.150705592T>G	GRCh37
NC_000001.9:g.148972216T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.926A>C MANE Select	ENSP00000357981.3:p.Tyr309Ser
ENST00000448301.7:c.698A>C	ENSP00000408414.2:p.Tyr233Ser
ENST00000472977.7:c.926A>C	ENSP00000475176.2:p.Tyr309Ser
ENST00000483930.2:c.*120A>C	ENSP00000475812.2:n.*120A>C
ENST00000607427.2:c.926A>C	ENSP00000475557.2:p.Tyr309Ser
ENST00000679512.1:c.823A>C	ENSP00000505113.1:p.Ile275Leu
ENST00000679898.1:c.653A>C	ENSP00000505326.1:p.Tyr218Ser
ENST00000680288.1:c.776A>C	ENSP00000506001.1:p.Tyr259Ser
ENST00000680311.1:c.*9A>C	ENSP00000505020.1:n.*9A>C
ENST00000680471.1:c.*97A>C	ENSP00000506603.1:n.*97A>C
ENST00000680664.1:c.749A>C	ENSP00000506248.1:p.Tyr250Ser
ENST00000680931.1:c.*276A>C	ENSP00000504934.1:n.*276A>C
ENST00000681357.1:n.316A>C
ENST00000681444.1:c.926A>C	ENSP00000505359.1:p.Tyr309Ser
ENST00000368985.7:c.926A>C	ENSP00000357981.3:p.Tyr309Ser
ENST00000448301.6:c.776A>C	ENSP00000408414.1:p.Tyr259Ser
ENST00000472977.6:c.219A>C
ENST00000483930.1:c.474A>C	ENSP00000475812.1:n.474A>C
NM_001199739.1:c.776A>C	NP_001186668.1:p.Tyr259Ser
NM_004079.4:c.926A>C	NP_004070.3:p.Tyr309Ser
NM_004079.5:c.926A>C MANE Select	NP_004070.3:p.Tyr309Ser
NM_001199739.2:c.776A>C	NP_001186668.1:p.Tyr259Ser