Canonical Allele Identifier: CA2479286207

Gene: CTSS

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.907A= MANE Select	ENSP00000357981.3:p.Asn303=
ENST00000448301.7:c.679A=	ENSP00000408414.2:p.Asn227=
ENST00000472977.7:c.907A=	ENSP00000475176.2:p.Asn303=
ENST00000483930.2:c.*101A=	ENSP00000475812.2:n.*101A=
ENST00000607427.2:c.907A=	ENSP00000475557.2:p.Asn303=
ENST00000679512.1:c.804A=	ENSP00000505113.1:p.Thr268=
ENST00000679898.1:c.634A=	ENSP00000505326.1:p.Asn212=
ENST00000680288.1:c.757A=	ENSP00000506001.1:p.Asn253=
ENST00000680311.1:c.638A=	ENSP00000505020.1:p.Gln213=
ENST00000680471.1:c.*78A=	ENSP00000506603.1:n.*78A=
ENST00000680664.1:c.730A=	ENSP00000506248.1:p.Asn244=
ENST00000680931.1:c.*257A=	ENSP00000504934.1:n.*257A=
ENST00000681357.1:n.297A=
ENST00000681444.1:c.907A=	ENSP00000505359.1:p.Asn303=
ENST00000368985.7:c.907A=	ENSP00000357981.3:p.Asn303=
ENST00000448301.6:c.757A=	ENSP00000408414.1:p.Asn253=
ENST00000472977.6:c.200A=
ENST00000483930.1:c.455A=	ENSP00000475812.1:n.455A=
NM_001199739.1:c.757A=	NP_001186668.1:p.Asn253=
NM_004079.4:c.907A=	NP_004070.3:p.Asn303=
NM_004079.5:c.907A= MANE Select	NP_004070.3:p.Asn303=
NM_001199739.2:c.757A=	NP_001186668.1:p.Asn253=