Canonical Allele Identifier: CA420696564

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705567T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733091T>C , CM000663.2:g.150733091T>C	GRCh38
NC_000001.10:g.150705567T>C , CM000663.1:g.150705567T>C	GRCh37
NC_000001.9:g.148972191T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.951A>G MANE Select	ENSP00000357981.3:p.Gly317=
ENST00000448301.7:c.723A>G	ENSP00000408414.2:p.Gly241=
ENST00000472977.7:c.951A>G	ENSP00000475176.2:p.Gly317=
ENST00000483930.2:c.*145A>G	ENSP00000475812.2:n.*145A>G
ENST00000607427.2:c.951A>G	ENSP00000475557.2:p.Gly317=
ENST00000679512.1:c.848A>G	ENSP00000505113.1:p.Glu283Gly
ENST00000679898.1:c.678A>G	ENSP00000505326.1:p.Gly226=
ENST00000680288.1:c.801A>G	ENSP00000506001.1:p.Gly267=
ENST00000680311.1:c.*34A>G	ENSP00000505020.1:n.*34A>G
ENST00000680471.1:c.*122A>G	ENSP00000506603.1:n.*122A>G
ENST00000680664.1:c.774A>G	ENSP00000506248.1:p.Gly258=
ENST00000680931.1:c.*301A>G	ENSP00000504934.1:n.*301A>G
ENST00000681357.1:n.341A>G
ENST00000681444.1:c.951A>G	ENSP00000505359.1:p.Gly317=
ENST00000368985.7:c.951A>G	ENSP00000357981.3:p.Gly317=
ENST00000448301.6:c.801A>G	ENSP00000408414.1:p.Gly267=
ENST00000472977.6:c.244A>G
ENST00000483930.1:c.499A>G	ENSP00000475812.1:n.499A>G
NM_001199739.1:c.801A>G	NP_001186668.1:p.Gly267=
NM_004079.4:c.951A>G	NP_004070.3:p.Gly317=
NM_004079.5:c.951A>G MANE Select	NP_004070.3:p.Gly317=
NM_001199739.2:c.801A>G	NP_001186668.1:p.Gly267=