Canonical Allele Identifier: CA342322449

Gene: CTSS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.923G>T MANE Select	ENSP00000357981.3:p.Gly308Val
ENST00000448301.7:c.695G>T	ENSP00000408414.2:p.Gly232Val
ENST00000472977.7:c.923G>T	ENSP00000475176.2:p.Gly308Val
ENST00000483930.2:c.*117G>T	ENSP00000475812.2:n.*117G>T
ENST00000607427.2:c.923G>T	ENSP00000475557.2:p.Gly308Val
ENST00000679512.1:c.820G>T	ENSP00000505113.1:p.Asp274Tyr
ENST00000679898.1:c.650G>T	ENSP00000505326.1:p.Gly217Val
ENST00000680288.1:c.773G>T	ENSP00000506001.1:p.Gly258Val
ENST00000680311.1:c.*6G>T	ENSP00000505020.1:n.*6G>T
ENST00000680471.1:c.*94G>T	ENSP00000506603.1:n.*94G>T
ENST00000680664.1:c.746G>T	ENSP00000506248.1:p.Gly249Val
ENST00000680931.1:c.*273G>T	ENSP00000504934.1:n.*273G>T
ENST00000681357.1:n.313G>T
ENST00000681444.1:c.923G>T	ENSP00000505359.1:p.Gly308Val
ENST00000368985.7:c.923G>T	ENSP00000357981.3:p.Gly308Val
ENST00000448301.6:c.773G>T	ENSP00000408414.1:p.Gly258Val
ENST00000472977.6:c.216G>T
ENST00000483930.1:c.471G>T	ENSP00000475812.1:n.471G>T
NM_001199739.1:c.773G>T	NP_001186668.1:p.Gly258Val
NM_004079.4:c.923G>T	NP_004070.3:p.Gly308Val
NM_004079.5:c.923G>T MANE Select	NP_004070.3:p.Gly308Val
NM_001199739.2:c.773G>T	NP_001186668.1:p.Gly258Val