Canonical Allele Identifier: CA342322499

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705614G>T (hg19) ; chr1:g.150733138G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733138G>T , CM000663.2:g.150733138G>T	GRCh38
NC_000001.10:g.150705614G>T , CM000663.1:g.150705614G>T	GRCh37
NC_000001.9:g.148972238G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.904C>A MANE Select	ENSP00000357981.3:p.His302Asn
ENST00000448301.7:c.676C>A	ENSP00000408414.2:p.His226Asn
ENST00000472977.7:c.904C>A	ENSP00000475176.2:p.His302Asn
ENST00000483930.2:c.*98C>A	ENSP00000475812.2:n.*98C>A
ENST00000607427.2:c.904C>A	ENSP00000475557.2:p.His302Asn
ENST00000679512.1:c.801C>A	ENSP00000505113.1:p.Ala267=
ENST00000679898.1:c.631C>A	ENSP00000505326.1:p.His211Asn
ENST00000680288.1:c.754C>A	ENSP00000506001.1:p.His252Asn
ENST00000680311.1:c.635C>A	ENSP00000505020.1:p.Pro212Gln
ENST00000680471.1:c.*75C>A	ENSP00000506603.1:n.*75C>A
ENST00000680664.1:c.727C>A	ENSP00000506248.1:p.His243Asn
ENST00000680931.1:c.*254C>A	ENSP00000504934.1:n.*254C>A
ENST00000681357.1:n.294C>A
ENST00000681444.1:c.904C>A	ENSP00000505359.1:p.His302Asn
ENST00000368985.7:c.904C>A	ENSP00000357981.3:p.His302Asn
ENST00000448301.6:c.754C>A	ENSP00000408414.1:p.His252Asn
ENST00000472977.6:c.197C>A
ENST00000483930.1:c.452C>A	ENSP00000475812.1:n.452C>A
NM_001199739.1:c.754C>A	NP_001186668.1:p.His252Asn
NM_004079.4:c.904C>A	NP_004070.3:p.His302Asn
NM_004079.5:c.904C>A MANE Select	NP_004070.3:p.His302Asn
NM_001199739.2:c.754C>A	NP_001186668.1:p.His252Asn