Canonical Allele Identifier: CA342322409

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705575T>G (hg19) ; chr1:g.150733099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733099T>G , CM000663.2:g.150733099T>G	GRCh38
NC_000001.10:g.150705575T>G , CM000663.1:g.150705575T>G	GRCh37
NC_000001.9:g.148972199T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.943A>C MANE Select	ENSP00000357981.3:p.Asn315His
ENST00000448301.7:c.715A>C	ENSP00000408414.2:p.Asn239His
ENST00000472977.7:c.943A>C	ENSP00000475176.2:p.Asn315His
ENST00000483930.2:c.*137A>C	ENSP00000475812.2:n.*137A>C
ENST00000607427.2:c.943A>C	ENSP00000475557.2:p.Asn315His
ENST00000679512.1:c.840A>C	ENSP00000505113.1:p.Glu280Asp
ENST00000679898.1:c.670A>C	ENSP00000505326.1:p.Asn224His
ENST00000680288.1:c.793A>C	ENSP00000506001.1:p.Asn265His
ENST00000680311.1:c.*26A>C	ENSP00000505020.1:n.*26A>C
ENST00000680471.1:c.*114A>C	ENSP00000506603.1:n.*114A>C
ENST00000680664.1:c.766A>C	ENSP00000506248.1:p.Asn256His
ENST00000680931.1:c.*293A>C	ENSP00000504934.1:n.*293A>C
ENST00000681357.1:n.333A>C
ENST00000681444.1:c.943A>C	ENSP00000505359.1:p.Asn315His
ENST00000368985.7:c.943A>C	ENSP00000357981.3:p.Asn315His
ENST00000448301.6:c.793A>C	ENSP00000408414.1:p.Asn265His
ENST00000472977.6:c.236A>C
ENST00000483930.1:c.491A>C	ENSP00000475812.1:n.491A>C
NM_001199739.1:c.793A>C	NP_001186668.1:p.Asn265His
NM_004079.4:c.943A>C	NP_004070.3:p.Asn315His
NM_004079.5:c.943A>C MANE Select	NP_004070.3:p.Asn315His
NM_001199739.2:c.793A>C	NP_001186668.1:p.Asn265His