Canonical Allele Identifier: CA342322487

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705610T>A (hg19) ; chr1:g.150733134T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733134T>A , CM000663.2:g.150733134T>A	GRCh38
NC_000001.10:g.150705610T>A , CM000663.1:g.150705610T>A	GRCh37
NC_000001.9:g.148972234T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.908A>T MANE Select	ENSP00000357981.3:p.Asn303Ile
ENST00000448301.7:c.680A>T	ENSP00000408414.2:p.Asn227Ile
ENST00000472977.7:c.908A>T	ENSP00000475176.2:p.Asn303Ile
ENST00000483930.2:c.*102A>T	ENSP00000475812.2:n.*102A>T
ENST00000607427.2:c.908A>T	ENSP00000475557.2:p.Asn303Ile
ENST00000679512.1:c.805A>T	ENSP00000505113.1:p.Thr269Ser
ENST00000679898.1:c.635A>T	ENSP00000505326.1:p.Asn212Ile
ENST00000680288.1:c.758A>T	ENSP00000506001.1:p.Asn253Ile
ENST00000680311.1:c.639A>T	ENSP00000505020.1:p.Gln213His
ENST00000680471.1:c.*79A>T	ENSP00000506603.1:n.*79A>T
ENST00000680664.1:c.731A>T	ENSP00000506248.1:p.Asn244Ile
ENST00000680931.1:c.*258A>T	ENSP00000504934.1:n.*258A>T
ENST00000681357.1:n.298A>T
ENST00000681444.1:c.908A>T	ENSP00000505359.1:p.Asn303Ile
ENST00000368985.7:c.908A>T	ENSP00000357981.3:p.Asn303Ile
ENST00000448301.6:c.758A>T	ENSP00000408414.1:p.Asn253Ile
ENST00000472977.6:c.201A>T
ENST00000483930.1:c.456A>T	ENSP00000475812.1:n.456A>T
NM_001199739.1:c.758A>T	NP_001186668.1:p.Asn253Ile
NM_004079.4:c.908A>T	NP_004070.3:p.Asn303Ile
NM_004079.5:c.908A>T MANE Select	NP_004070.3:p.Asn303Ile
NM_001199739.2:c.758A>T	NP_001186668.1:p.Asn253Ile