Canonical Allele Identifier: CA342322440

Gene: CTSS

Linked Data

• dbSNP Id: rs2101907274
• MyVariant Identifiers: chr1:g.150705590T>C (hg19) ; chr1:g.150733114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733114T>C , CM000663.2:g.150733114T>C	GRCh38
NC_000001.10:g.150705590T>C , CM000663.1:g.150705590T>C	GRCh37
NC_000001.9:g.148972214T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.928A>G MANE Select	ENSP00000357981.3:p.Ile310Val
ENST00000448301.7:c.700A>G	ENSP00000408414.2:p.Ile234Val
ENST00000472977.7:c.928A>G	ENSP00000475176.2:p.Ile310Val
ENST00000483930.2:c.*122A>G	ENSP00000475812.2:n.*122A>G
ENST00000607427.2:c.928A>G	ENSP00000475557.2:p.Ile310Val
ENST00000679512.1:c.825A>G	ENSP00000505113.1:p.Ile275Met
ENST00000679898.1:c.655A>G	ENSP00000505326.1:p.Ile219Val
ENST00000680288.1:c.778A>G	ENSP00000506001.1:p.Ile260Val
ENST00000680311.1:c.*11A>G	ENSP00000505020.1:n.*11A>G
ENST00000680471.1:c.*99A>G	ENSP00000506603.1:n.*99A>G
ENST00000680664.1:c.751A>G	ENSP00000506248.1:p.Ile251Val
ENST00000680931.1:c.*278A>G	ENSP00000504934.1:n.*278A>G
ENST00000681357.1:n.318A>G
ENST00000681444.1:c.928A>G	ENSP00000505359.1:p.Ile310Val
ENST00000368985.7:c.928A>G	ENSP00000357981.3:p.Ile310Val
ENST00000448301.6:c.778A>G	ENSP00000408414.1:p.Ile260Val
ENST00000472977.6:c.221A>G
ENST00000483930.1:c.476A>G	ENSP00000475812.1:n.476A>G
NM_001199739.1:c.778A>G	NP_001186668.1:p.Ile260Val
NM_004079.4:c.928A>G	NP_004070.3:p.Ile310Val
NM_004079.5:c.928A>G MANE Select	NP_004070.3:p.Ile310Val
NM_001199739.2:c.778A>G	NP_001186668.1:p.Ile260Val