Canonical Allele Identifier: CA342322421

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705581C>G (hg19) ; chr1:g.150733105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733105C>G , CM000663.2:g.150733105C>G	GRCh38
NC_000001.10:g.150705581C>G , CM000663.1:g.150705581C>G	GRCh37
NC_000001.9:g.148972205C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.937G>C MANE Select	ENSP00000357981.3:p.Ala313Pro
ENST00000448301.7:c.709G>C	ENSP00000408414.2:p.Ala237Pro
ENST00000472977.7:c.937G>C	ENSP00000475176.2:p.Ala313Pro
ENST00000483930.2:c.*131G>C	ENSP00000475812.2:n.*131G>C
ENST00000607427.2:c.937G>C	ENSP00000475557.2:p.Ala313Pro
ENST00000679512.1:c.834G>C	ENSP00000505113.1:p.Trp278Cys
ENST00000679898.1:c.664G>C	ENSP00000505326.1:p.Ala222Pro
ENST00000680288.1:c.787G>C	ENSP00000506001.1:p.Ala263Pro
ENST00000680311.1:c.*20G>C	ENSP00000505020.1:n.*20G>C
ENST00000680471.1:c.*108G>C	ENSP00000506603.1:n.*108G>C
ENST00000680664.1:c.760G>C	ENSP00000506248.1:p.Ala254Pro
ENST00000680931.1:c.*287G>C	ENSP00000504934.1:n.*287G>C
ENST00000681357.1:n.327G>C
ENST00000681444.1:c.937G>C	ENSP00000505359.1:p.Ala313Pro
ENST00000368985.7:c.937G>C	ENSP00000357981.3:p.Ala313Pro
ENST00000448301.6:c.787G>C	ENSP00000408414.1:p.Ala263Pro
ENST00000472977.6:c.230G>C
ENST00000483930.1:c.485G>C	ENSP00000475812.1:n.485G>C
NM_001199739.1:c.787G>C	NP_001186668.1:p.Ala263Pro
NM_004079.4:c.937G>C	NP_004070.3:p.Ala313Pro
NM_004079.5:c.937G>C MANE Select	NP_004070.3:p.Ala313Pro
NM_001199739.2:c.787G>C	NP_001186668.1:p.Ala263Pro