Canonical Allele Identifier: CA342322496

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733137-T-G
• MyVariant Identifiers: chr1:g.150705613T>G (hg19) ; chr1:g.150733137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733137T>G , CM000663.2:g.150733137T>G	GRCh38
NC_000001.10:g.150705613T>G , CM000663.1:g.150705613T>G	GRCh37
NC_000001.9:g.148972237T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.905A>C MANE Select	ENSP00000357981.3:p.His302Pro
ENST00000448301.7:c.677A>C	ENSP00000408414.2:p.His226Pro
ENST00000472977.7:c.905A>C	ENSP00000475176.2:p.His302Pro
ENST00000483930.2:c.*99A>C	ENSP00000475812.2:n.*99A>C
ENST00000607427.2:c.905A>C	ENSP00000475557.2:p.His302Pro
ENST00000679512.1:c.802A>C	ENSP00000505113.1:p.Thr268Pro
ENST00000679898.1:c.632A>C	ENSP00000505326.1:p.His211Pro
ENST00000680288.1:c.755A>C	ENSP00000506001.1:p.His252Pro
ENST00000680311.1:c.636A>C	ENSP00000505020.1:p.Pro212=
ENST00000680471.1:c.*76A>C	ENSP00000506603.1:n.*76A>C
ENST00000680664.1:c.728A>C	ENSP00000506248.1:p.His243Pro
ENST00000680931.1:c.*255A>C	ENSP00000504934.1:n.*255A>C
ENST00000681357.1:n.295A>C
ENST00000681444.1:c.905A>C	ENSP00000505359.1:p.His302Pro
ENST00000368985.7:c.905A>C	ENSP00000357981.3:p.His302Pro
ENST00000448301.6:c.755A>C	ENSP00000408414.1:p.His252Pro
ENST00000472977.6:c.198A>C
ENST00000483930.1:c.453A>C	ENSP00000475812.1:n.453A>C
NM_001199739.1:c.755A>C	NP_001186668.1:p.His252Pro
NM_004079.4:c.905A>C	NP_004070.3:p.His302Pro
NM_004079.5:c.905A>C MANE Select	NP_004070.3:p.His302Pro
NM_001199739.2:c.755A>C	NP_001186668.1:p.His252Pro