Canonical Allele Identifier: CA526062656

Gene: CTSS

Linked Data

• dbSNP Id: rs1011769905
• gnomAD v2: 1-150705480-G-C
• gnomAD v4: 1-150733004-G-C
• MyVariant Identifiers: chr1:g.150705480G>C (hg19) ; chr1:g.150733004G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733004G>C , CM000663.2:g.150733004G>C	GRCh38
NC_000001.10:g.150705480G>C , CM000663.1:g.150705480G>C	GRCh37
NC_000001.9:g.148972104G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*42C>G MANE Select	ENSP00000357981.3:n.*42C>G
ENST00000448301.7:c.*42C>G	ENSP00000408414.2:n.*42C>G
ENST00000472977.7:c.*42C>G	ENSP00000475176.2:n.*42C>G
ENST00000483930.2:c.*232C>G	ENSP00000475812.2:n.*232C>G
ENST00000607427.2:c.*42C>G	ENSP00000475557.2:n.*42C>G
ENST00000679512.1:c.*5C>G	ENSP00000505113.1:n.*5C>G
ENST00000679898.1:c.*42C>G	ENSP00000505326.1:n.*42C>G
ENST00000680288.1:c.*42C>G	ENSP00000506001.1:n.*42C>G
ENST00000680311.1:c.*121C>G	ENSP00000505020.1:n.*121C>G
ENST00000680471.1:c.*209C>G	ENSP00000506603.1:n.*209C>G
ENST00000680664.1:c.*42C>G	ENSP00000506248.1:n.*42C>G
ENST00000680931.1:c.*388C>G	ENSP00000504934.1:n.*388C>G
ENST00000681357.1:n.428C>G
ENST00000681444.1:c.*42C>G	ENSP00000505359.1:n.*42C>G
ENST00000368985.7:c.*42C>G	ENSP00000357981.3:n.*42C>G
ENST00000448301.6:c.*42C>G	ENSP00000408414.1:n.*42C>G
ENST00000472977.6:c.331C>G
ENST00000483930.1:c.586C>G	ENSP00000475812.1:n.586C>G
ENST00000607427.1:c.59C>G
NM_001199739.1:c.*42C>G	NP_001186668.1:n.*42C>G
NM_004079.4:c.*42C>G	NP_004070.3:n.*42C>G
NM_004079.5:c.*42C>G MANE Select	NP_004070.3:n.*42C>G
NM_001199739.2:c.*42C>G	NP_001186668.1:n.*42C>G