Canonical Allele Identifier: CA342322491

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705611T>A (hg19) ; chr1:g.150733135T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733135T>A , CM000663.2:g.150733135T>A	GRCh38
NC_000001.10:g.150705611T>A , CM000663.1:g.150705611T>A	GRCh37
NC_000001.9:g.148972235T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.907A>T MANE Select	ENSP00000357981.3:p.Asn303Tyr
ENST00000448301.7:c.679A>T	ENSP00000408414.2:p.Asn227Tyr
ENST00000472977.7:c.907A>T	ENSP00000475176.2:p.Asn303Tyr
ENST00000483930.2:c.*101A>T	ENSP00000475812.2:n.*101A>T
ENST00000607427.2:c.907A>T	ENSP00000475557.2:p.Asn303Tyr
ENST00000679512.1:c.804A>T	ENSP00000505113.1:p.Thr268=
ENST00000679898.1:c.634A>T	ENSP00000505326.1:p.Asn212Tyr
ENST00000680288.1:c.757A>T	ENSP00000506001.1:p.Asn253Tyr
ENST00000680311.1:c.638A>T	ENSP00000505020.1:p.Gln213Leu
ENST00000680471.1:c.*78A>T	ENSP00000506603.1:n.*78A>T
ENST00000680664.1:c.730A>T	ENSP00000506248.1:p.Asn244Tyr
ENST00000680931.1:c.*257A>T	ENSP00000504934.1:n.*257A>T
ENST00000681357.1:n.297A>T
ENST00000681444.1:c.907A>T	ENSP00000505359.1:p.Asn303Tyr
ENST00000368985.7:c.907A>T	ENSP00000357981.3:p.Asn303Tyr
ENST00000448301.6:c.757A>T	ENSP00000408414.1:p.Asn253Tyr
ENST00000472977.6:c.200A>T
ENST00000483930.1:c.455A>T	ENSP00000475812.1:n.455A>T
NM_001199739.1:c.757A>T	NP_001186668.1:p.Asn253Tyr
NM_004079.4:c.907A>T	NP_004070.3:p.Asn303Tyr
NM_004079.5:c.907A>T MANE Select	NP_004070.3:p.Asn303Tyr
NM_001199739.2:c.757A>T	NP_001186668.1:p.Asn253Tyr