Canonical Allele Identifier: CA1143536865

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733094T= , CM000663.2:g.150733094T=	GRCh38
NC_000001.10:g.150705570T= , CM000663.1:g.150705570T=	GRCh37
NC_000001.9:g.148972194T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.948A= MANE Select	ENSP00000357981.3:p.Lys316=
ENST00000448301.7:c.720A=	ENSP00000408414.2:p.Lys240=
ENST00000472977.7:c.948A=	ENSP00000475176.2:p.Lys316=
ENST00000483930.2:c.*142A=	ENSP00000475812.2:n.*142A=
ENST00000607427.2:c.948A=	ENSP00000475557.2:p.Lys316=
ENST00000679512.1:c.845A=	ENSP00000505113.1:p.Lys282=
ENST00000679898.1:c.675A=	ENSP00000505326.1:p.Lys225=
ENST00000680288.1:c.798A=	ENSP00000506001.1:p.Lys266=
ENST00000680311.1:c.*31A=	ENSP00000505020.1:n.*31A=
ENST00000680471.1:c.*119A=	ENSP00000506603.1:n.*119A=
ENST00000680664.1:c.771A=	ENSP00000506248.1:p.Lys257=
ENST00000680931.1:c.*298A=	ENSP00000504934.1:n.*298A=
ENST00000681357.1:n.338A=
ENST00000681444.1:c.948A=	ENSP00000505359.1:p.Lys316=
ENST00000368985.7:c.948A=	ENSP00000357981.3:p.Lys316=
ENST00000448301.6:c.798A=	ENSP00000408414.1:p.Lys266=
ENST00000472977.6:c.241A=
ENST00000483930.1:c.496A=	ENSP00000475812.1:n.496A=
NM_001199739.1:c.798A=	NP_001186668.1:p.Lys266=
NM_004079.4:c.948A=	NP_004070.3:p.Lys316=
NM_004079.5:c.948A= MANE Select	NP_004070.3:p.Lys316=
NM_001199739.2:c.798A=	NP_001186668.1:p.Lys266=