Canonical Allele Identifier: CA420696592

Gene: CTSS

Linked Data

• gnomAD v4: 1-150733145-G-A
• MyVariant Identifiers: chr1:g.150705621G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733145G>A , CM000663.2:g.150733145G>A	GRCh38
NC_000001.10:g.150705621G>A , CM000663.1:g.150705621G>A	GRCh37
NC_000001.9:g.148972245G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897C>T MANE Select	ENSP00000357981.3:p.Ser299=
ENST00000448301.7:c.669C>T	ENSP00000408414.2:p.Ser223=
ENST00000472977.7:c.897C>T	ENSP00000475176.2:p.Ser299=
ENST00000483930.2:c.*91C>T	ENSP00000475812.2:n.*91C>T
ENST00000607427.2:c.897C>T	ENSP00000475557.2:p.Ser299=
ENST00000679512.1:c.794C>T	ENSP00000505113.1:p.Ala265Val
ENST00000679898.1:c.624C>T	ENSP00000505326.1:p.Ser208=
ENST00000680288.1:c.747C>T	ENSP00000506001.1:p.Ser249=
ENST00000680311.1:c.628C>T	ENSP00000505020.1:p.Leu210=
ENST00000680471.1:c.*68C>T	ENSP00000506603.1:n.*68C>T
ENST00000680664.1:c.720C>T	ENSP00000506248.1:p.Ser240=
ENST00000680931.1:c.*247C>T	ENSP00000504934.1:n.*247C>T
ENST00000681357.1:n.287C>T
ENST00000681444.1:c.897C>T	ENSP00000505359.1:p.Ser299=
ENST00000368985.7:c.897C>T	ENSP00000357981.3:p.Ser299=
ENST00000448301.6:c.747C>T	ENSP00000408414.1:p.Ser249=
ENST00000472977.6:c.190C>T
ENST00000483930.1:c.445C>T	ENSP00000475812.1:n.445C>T
NM_001199739.1:c.747C>T	NP_001186668.1:p.Ser249=
NM_004079.4:c.897C>T	NP_004070.3:p.Ser299=
NM_004079.5:c.897C>T MANE Select	NP_004070.3:p.Ser299=
NM_001199739.2:c.747C>T	NP_001186668.1:p.Ser249=