Canonical Allele Identifier: CA889264217

Gene: CTSS

Linked Data

• dbSNP Id: rs1207500750
• MyVariant Identifiers: chr1:g.150705850T>C (hg19) ; chr1:g.150733374T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733374T>C , CM000663.2:g.150733374T>C	GRCh38
NC_000001.10:g.150705850T>C , CM000663.1:g.150705850T>C	GRCh37
NC_000001.9:g.148972474T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897-229A>G MANE Select	ENSP00000357981.3:n.897-229A>G
ENST00000448301.7:c.669-229A>G	ENSP00000408414.2:n.669-229A>G
ENST00000472977.7:c.897-229A>G	ENSP00000475176.2:n.897-229A>G
ENST00000483930.2:c.*91-229A>G	ENSP00000475812.2:n.*91-229A>G
ENST00000607427.2:c.897-229A>G	ENSP00000475557.2:n.897-229A>G
ENST00000679512.1:c.794-229A>G	ENSP00000505113.1:n.794-229A>G
ENST00000679898.1:c.624-229A>G	ENSP00000505326.1:n.624-229A>G
ENST00000680288.1:c.747-229A>G	ENSP00000506001.1:n.747-229A>G
ENST00000680311.1:c.628-229A>G	ENSP00000505020.1:n.628-229A>G
ENST00000680471.1:c.*68-229A>G	ENSP00000506603.1:n.*68-229A>G
ENST00000680664.1:c.720-229A>G	ENSP00000506248.1:n.720-229A>G
ENST00000680931.1:c.*247-229A>G	ENSP00000504934.1:n.*247-229A>G
ENST00000681357.1:n.287-229A>G
ENST00000681444.1:c.897-229A>G	ENSP00000505359.1:n.897-229A>G
ENST00000368985.7:c.897-229A>G	ENSP00000357981.3:n.897-229A>G
ENST00000448301.6:c.747-229A>G	ENSP00000408414.1:n.747-229A>G
ENST00000472977.6:c.190-229A>G
ENST00000483930.1:c.445-229A>G	ENSP00000475812.1:n.445-229A>G
NM_001199739.1:c.747-229A>G	NP_001186668.1:n.747-229A>G
NM_004079.4:c.897-229A>G	NP_004070.3:n.897-229A>G
NM_004079.5:c.897-229A>G MANE Select	NP_004070.3:n.897-229A>G
NM_001199739.2:c.747-229A>G	NP_001186668.1:n.747-229A>G