Canonical Allele Identifier: CA420696582

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705594T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733118T>G , CM000663.2:g.150733118T>G	GRCh38
NC_000001.10:g.150705594T>G , CM000663.1:g.150705594T>G	GRCh37
NC_000001.9:g.148972218T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.924A>C MANE Select	ENSP00000357981.3:p.Gly308=
ENST00000448301.7:c.696A>C	ENSP00000408414.2:p.Gly232=
ENST00000472977.7:c.924A>C	ENSP00000475176.2:p.Gly308=
ENST00000483930.2:c.*118A>C	ENSP00000475812.2:n.*118A>C
ENST00000607427.2:c.924A>C	ENSP00000475557.2:p.Gly308=
ENST00000679512.1:c.821A>C	ENSP00000505113.1:p.Asp274Ala
ENST00000679898.1:c.651A>C	ENSP00000505326.1:p.Gly217=
ENST00000680288.1:c.774A>C	ENSP00000506001.1:p.Gly258=
ENST00000680311.1:c.*7A>C	ENSP00000505020.1:n.*7A>C
ENST00000680471.1:c.*95A>C	ENSP00000506603.1:n.*95A>C
ENST00000680664.1:c.747A>C	ENSP00000506248.1:p.Gly249=
ENST00000680931.1:c.*274A>C	ENSP00000504934.1:n.*274A>C
ENST00000681357.1:n.314A>C
ENST00000681444.1:c.924A>C	ENSP00000505359.1:p.Gly308=
ENST00000368985.7:c.924A>C	ENSP00000357981.3:p.Gly308=
ENST00000448301.6:c.774A>C	ENSP00000408414.1:p.Gly258=
ENST00000472977.6:c.217A>C
ENST00000483930.1:c.472A>C	ENSP00000475812.1:n.472A>C
NM_001199739.1:c.774A>C	NP_001186668.1:p.Gly258=
NM_004079.4:c.924A>C	NP_004070.3:p.Gly308=
NM_004079.5:c.924A>C MANE Select	NP_004070.3:p.Gly308=
NM_001199739.2:c.774A>C	NP_001186668.1:p.Gly258=