Canonical Allele Identifier: CA526062664

Gene: CTSS

Linked Data

• dbSNP Id: rs1264871061
• gnomAD v2: 1-150705486-C-T
• gnomAD v3: 1-150733010-C-T
• gnomAD v4: 1-150733010-C-T
• MyVariant Identifiers: chr1:g.150705486C>T (hg19) ; chr1:g.150733010C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733010C>T , CM000663.2:g.150733010C>T	GRCh38
NC_000001.10:g.150705486C>T , CM000663.1:g.150705486C>T	GRCh37
NC_000001.9:g.148972110C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*36G>A MANE Select	ENSP00000357981.3:n.*36G>A
ENST00000448301.7:c.*36G>A	ENSP00000408414.2:n.*36G>A
ENST00000472977.7:c.*36G>A	ENSP00000475176.2:n.*36G>A
ENST00000483930.2:c.*226G>A	ENSP00000475812.2:n.*226G>A
ENST00000607427.2:c.*36G>A	ENSP00000475557.2:n.*36G>A
ENST00000679512.1:c.929G>A	ENSP00000505113.1:p.Ter310=
ENST00000679898.1:c.*36G>A	ENSP00000505326.1:n.*36G>A
ENST00000680288.1:c.*36G>A	ENSP00000506001.1:n.*36G>A
ENST00000680311.1:c.*115G>A	ENSP00000505020.1:n.*115G>A
ENST00000680471.1:c.*203G>A	ENSP00000506603.1:n.*203G>A
ENST00000680664.1:c.*36G>A	ENSP00000506248.1:n.*36G>A
ENST00000680931.1:c.*382G>A	ENSP00000504934.1:n.*382G>A
ENST00000681357.1:n.422G>A
ENST00000681444.1:c.*36G>A	ENSP00000505359.1:n.*36G>A
ENST00000368985.7:c.*36G>A	ENSP00000357981.3:n.*36G>A
ENST00000448301.6:c.*36G>A	ENSP00000408414.1:n.*36G>A
ENST00000472977.6:c.325G>A
ENST00000483930.1:c.580G>A	ENSP00000475812.1:n.580G>A
ENST00000607427.1:c.53G>A
NM_001199739.1:c.*36G>A	NP_001186668.1:n.*36G>A
NM_004079.4:c.*36G>A	NP_004070.3:n.*36G>A
NM_004079.5:c.*36G>A MANE Select	NP_004070.3:n.*36G>A
NM_001199739.2:c.*36G>A	NP_001186668.1:n.*36G>A