Canonical Allele Identifier: CA342322451

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705595C>G (hg19) ; chr1:g.150733119C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733119C>G , CM000663.2:g.150733119C>G	GRCh38
NC_000001.10:g.150705595C>G , CM000663.1:g.150705595C>G	GRCh37
NC_000001.9:g.148972219C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.923G>C MANE Select	ENSP00000357981.3:p.Gly308Ala
ENST00000448301.7:c.695G>C	ENSP00000408414.2:p.Gly232Ala
ENST00000472977.7:c.923G>C	ENSP00000475176.2:p.Gly308Ala
ENST00000483930.2:c.*117G>C	ENSP00000475812.2:n.*117G>C
ENST00000607427.2:c.923G>C	ENSP00000475557.2:p.Gly308Ala
ENST00000679512.1:c.820G>C	ENSP00000505113.1:p.Asp274His
ENST00000679898.1:c.650G>C	ENSP00000505326.1:p.Gly217Ala
ENST00000680288.1:c.773G>C	ENSP00000506001.1:p.Gly258Ala
ENST00000680311.1:c.*6G>C	ENSP00000505020.1:n.*6G>C
ENST00000680471.1:c.*94G>C	ENSP00000506603.1:n.*94G>C
ENST00000680664.1:c.746G>C	ENSP00000506248.1:p.Gly249Ala
ENST00000680931.1:c.*273G>C	ENSP00000504934.1:n.*273G>C
ENST00000681357.1:n.313G>C
ENST00000681444.1:c.923G>C	ENSP00000505359.1:p.Gly308Ala
ENST00000368985.7:c.923G>C	ENSP00000357981.3:p.Gly308Ala
ENST00000448301.6:c.773G>C	ENSP00000408414.1:p.Gly258Ala
ENST00000472977.6:c.216G>C
ENST00000483930.1:c.471G>C	ENSP00000475812.1:n.471G>C
NM_001199739.1:c.773G>C	NP_001186668.1:p.Gly258Ala
NM_004079.4:c.923G>C	NP_004070.3:p.Gly308Ala
NM_004079.5:c.923G>C MANE Select	NP_004070.3:p.Gly308Ala
NM_001199739.2:c.773G>C	NP_001186668.1:p.Gly258Ala