Canonical Allele Identifier: CA342322427

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705583A>G (hg19) ; chr1:g.150733107A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733107A>G , CM000663.2:g.150733107A>G	GRCh38
NC_000001.10:g.150705583A>G , CM000663.1:g.150705583A>G	GRCh37
NC_000001.9:g.148972207A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.935T>C MANE Select	ENSP00000357981.3:p.Met312Thr
ENST00000448301.7:c.707T>C	ENSP00000408414.2:p.Met236Thr
ENST00000472977.7:c.935T>C	ENSP00000475176.2:p.Met312Thr
ENST00000483930.2:c.*129T>C	ENSP00000475812.2:n.*129T>C
ENST00000607427.2:c.935T>C	ENSP00000475557.2:p.Met312Thr
ENST00000679512.1:c.832T>C	ENSP00000505113.1:p.Trp278Arg
ENST00000679898.1:c.662T>C	ENSP00000505326.1:p.Met221Thr
ENST00000680288.1:c.785T>C	ENSP00000506001.1:p.Met262Thr
ENST00000680311.1:c.*18T>C	ENSP00000505020.1:n.*18T>C
ENST00000680471.1:c.*106T>C	ENSP00000506603.1:n.*106T>C
ENST00000680664.1:c.758T>C	ENSP00000506248.1:p.Met253Thr
ENST00000680931.1:c.*285T>C	ENSP00000504934.1:n.*285T>C
ENST00000681357.1:n.325T>C
ENST00000681444.1:c.935T>C	ENSP00000505359.1:p.Met312Thr
ENST00000368985.7:c.935T>C	ENSP00000357981.3:p.Met312Thr
ENST00000448301.6:c.785T>C	ENSP00000408414.1:p.Met262Thr
ENST00000472977.6:c.228T>C
ENST00000483930.1:c.483T>C	ENSP00000475812.1:n.483T>C
NM_001199739.1:c.785T>C	NP_001186668.1:p.Met262Thr
NM_004079.4:c.935T>C	NP_004070.3:p.Met312Thr
NM_004079.5:c.935T>C MANE Select	NP_004070.3:p.Met312Thr
NM_001199739.2:c.785T>C	NP_001186668.1:p.Met262Thr