Canonical Allele Identifier: CA342327407

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150722592G>T (hg19) ; chr1:g.150750116G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150750116G>T , CM000663.2:g.150750116G>T	GRCh38
NC_000001.10:g.150722592G>T , CM000663.1:g.150722592G>T	GRCh37
NC_000001.9:g.148989216G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.683C>A MANE Select	ENSP00000357981.3:p.Thr228Asn
ENST00000448301.7:c.455C>A	ENSP00000408414.2:p.Thr152Asn
ENST00000472977.7:c.683C>A	ENSP00000475176.2:p.Thr228Asn
ENST00000483930.2:c.683C>A	ENSP00000475812.2:p.Thr228Asn
ENST00000607427.2:c.683C>A	ENSP00000475557.2:p.Thr228Asn
ENST00000679512.1:c.683C>A	ENSP00000505113.1:p.Thr228Asn
ENST00000679898.1:c.410C>A	ENSP00000505326.1:p.Thr137Asn
ENST00000680288.1:c.533C>A	ENSP00000506001.1:p.Thr178Asn
ENST00000680311.1:c.627+1665C>A	ENSP00000505020.1:n.627+1665C>A
ENST00000680471.1:c.627+1665C>A	ENSP00000506603.1:n.627+1665C>A
ENST00000680664.1:c.506C>A	ENSP00000506248.1:p.Thr169Asn
ENST00000680931.1:c.683C>A	ENSP00000504934.1:p.Thr228Asn
ENST00000681444.1:c.683C>A	ENSP00000505359.1:p.Thr228Asn
ENST00000681728.1:c.683C>A	ENSP00000505313.1:p.Thr228Asn
ENST00000368985.7:c.683C>A	ENSP00000357981.3:p.Thr228Asn
ENST00000448301.6:c.533C>A	ENSP00000408414.1:p.Thr178Asn
ENST00000480760.1:n.566+1665C>A
ENST00000483930.1:c.110C>A	ENSP00000475812.1:p.Thr37Asn
NM_001199739.1:c.533C>A	NP_001186668.1:p.Thr178Asn
NM_004079.4:c.683C>A	NP_004070.3:p.Thr228Asn
NM_004079.5:c.683C>A MANE Select	NP_004070.3:p.Thr228Asn
NM_001199739.2:c.533C>A	NP_001186668.1:p.Thr178Asn