Canonical Allele Identifier: CA420696591

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733139-G-T
• MyVariant Identifiers: chr1:g.150705615G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733139G>T , CM000663.2:g.150733139G>T	GRCh38
NC_000001.10:g.150705615G>T , CM000663.1:g.150705615G>T	GRCh37
NC_000001.9:g.148972239G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.903C>A MANE Select	ENSP00000357981.3:p.Gly301=
ENST00000448301.7:c.675C>A	ENSP00000408414.2:p.Gly225=
ENST00000472977.7:c.903C>A	ENSP00000475176.2:p.Gly301=
ENST00000483930.2:c.*97C>A	ENSP00000475812.2:n.*97C>A
ENST00000607427.2:c.903C>A	ENSP00000475557.2:p.Gly301=
ENST00000679512.1:c.800C>A	ENSP00000505113.1:p.Ala267Asp
ENST00000679898.1:c.630C>A	ENSP00000505326.1:p.Gly210=
ENST00000680288.1:c.753C>A	ENSP00000506001.1:p.Gly251=
ENST00000680311.1:c.634C>A	ENSP00000505020.1:p.Pro212Thr
ENST00000680471.1:c.*74C>A	ENSP00000506603.1:n.*74C>A
ENST00000680664.1:c.726C>A	ENSP00000506248.1:p.Gly242=
ENST00000680931.1:c.*253C>A	ENSP00000504934.1:n.*253C>A
ENST00000681357.1:n.293C>A
ENST00000681444.1:c.903C>A	ENSP00000505359.1:p.Gly301=
ENST00000368985.7:c.903C>A	ENSP00000357981.3:p.Gly301=
ENST00000448301.6:c.753C>A	ENSP00000408414.1:p.Gly251=
ENST00000472977.6:c.196C>A
ENST00000483930.1:c.451C>A	ENSP00000475812.1:n.451C>A
NM_001199739.1:c.753C>A	NP_001186668.1:p.Gly251=
NM_004079.4:c.903C>A	NP_004070.3:p.Gly301=
NM_004079.5:c.903C>A MANE Select	NP_004070.3:p.Gly301=
NM_001199739.2:c.753C>A	NP_001186668.1:p.Gly251=