Canonical Allele Identifier: CA342322480

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705607A>G (hg19) ; chr1:g.150733131A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733131A>G , CM000663.2:g.150733131A>G	GRCh38
NC_000001.10:g.150705607A>G , CM000663.1:g.150705607A>G	GRCh37
NC_000001.9:g.148972231A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.911T>C MANE Select	ENSP00000357981.3:p.Phe304Ser
ENST00000448301.7:c.683T>C	ENSP00000408414.2:p.Phe228Ser
ENST00000472977.7:c.911T>C	ENSP00000475176.2:p.Phe304Ser
ENST00000483930.2:c.*105T>C	ENSP00000475812.2:n.*105T>C
ENST00000607427.2:c.911T>C	ENSP00000475557.2:p.Phe304Ser
ENST00000679512.1:c.808T>C	ENSP00000505113.1:p.Leu270=
ENST00000679898.1:c.638T>C	ENSP00000505326.1:p.Phe213Ser
ENST00000680288.1:c.761T>C	ENSP00000506001.1:p.Phe254Ser
ENST00000680311.1:c.642T>C	ENSP00000505020.1:p.Leu214=
ENST00000680471.1:c.*82T>C	ENSP00000506603.1:n.*82T>C
ENST00000680664.1:c.734T>C	ENSP00000506248.1:p.Phe245Ser
ENST00000680931.1:c.*261T>C	ENSP00000504934.1:n.*261T>C
ENST00000681357.1:n.301T>C
ENST00000681444.1:c.911T>C	ENSP00000505359.1:p.Phe304Ser
ENST00000368985.7:c.911T>C	ENSP00000357981.3:p.Phe304Ser
ENST00000448301.6:c.761T>C	ENSP00000408414.1:p.Phe254Ser
ENST00000472977.6:c.204T>C
ENST00000483930.1:c.459T>C	ENSP00000475812.1:n.459T>C
NM_001199739.1:c.761T>C	NP_001186668.1:p.Phe254Ser
NM_004079.4:c.911T>C	NP_004070.3:p.Phe304Ser
NM_004079.5:c.911T>C MANE Select	NP_004070.3:p.Phe304Ser
NM_001199739.2:c.761T>C	NP_001186668.1:p.Phe254Ser