Canonical Allele Identifier: CA342322369

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733083-C-T
• MyVariant Identifiers: chr1:g.150705559C>T (hg19) ; chr1:g.150733083C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733083C>T , CM000663.2:g.150733083C>T	GRCh38
NC_000001.10:g.150705559C>T , CM000663.1:g.150705559C>T	GRCh37
NC_000001.9:g.148972183C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.959G>A MANE Select	ENSP00000357981.3:p.Cys320Tyr
ENST00000448301.7:c.731G>A	ENSP00000408414.2:p.Cys244Tyr
ENST00000472977.7:c.959G>A	ENSP00000475176.2:p.Cys320Tyr
ENST00000483930.2:c.*153G>A	ENSP00000475812.2:n.*153G>A
ENST00000607427.2:c.959G>A	ENSP00000475557.2:p.Cys320Tyr
ENST00000679512.1:c.856G>A	ENSP00000505113.1:p.Val286Met
ENST00000679898.1:c.686G>A	ENSP00000505326.1:p.Cys229Tyr
ENST00000680288.1:c.809G>A	ENSP00000506001.1:p.Cys270Tyr
ENST00000680311.1:c.*42G>A	ENSP00000505020.1:n.*42G>A
ENST00000680471.1:c.*130G>A	ENSP00000506603.1:n.*130G>A
ENST00000680664.1:c.782G>A	ENSP00000506248.1:p.Cys261Tyr
ENST00000680931.1:c.*309G>A	ENSP00000504934.1:n.*309G>A
ENST00000681357.1:n.349G>A
ENST00000681444.1:c.959G>A	ENSP00000505359.1:p.Cys320Tyr
ENST00000368985.7:c.959G>A	ENSP00000357981.3:p.Cys320Tyr
ENST00000448301.6:c.809G>A	ENSP00000408414.1:p.Cys270Tyr
ENST00000472977.6:c.252G>A
ENST00000483930.1:c.507G>A	ENSP00000475812.1:n.507G>A
NM_001199739.1:c.809G>A	NP_001186668.1:p.Cys270Tyr
NM_004079.4:c.959G>A	NP_004070.3:p.Cys320Tyr
NM_004079.5:c.959G>A MANE Select	NP_004070.3:p.Cys320Tyr
NM_001199739.2:c.809G>A	NP_001186668.1:p.Cys270Tyr