Canonical Allele Identifier: CA1007645435

Gene: CTSS

Linked Data

• dbSNP Id: rs1652565668
• gnomAD v3: 1-150733367-G-T
• gnomAD v4: 1-150733367-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733367G>T , CM000663.2:g.150733367G>T	GRCh38
NC_000001.10:g.150705843G>T , CM000663.1:g.150705843G>T	GRCh37
NC_000001.9:g.148972467G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897-222C>A MANE Select	ENSP00000357981.3:n.897-222C>A
ENST00000448301.7:c.669-222C>A	ENSP00000408414.2:n.669-222C>A
ENST00000472977.7:c.897-222C>A	ENSP00000475176.2:n.897-222C>A
ENST00000483930.2:c.*91-222C>A	ENSP00000475812.2:n.*91-222C>A
ENST00000607427.2:c.897-222C>A	ENSP00000475557.2:n.897-222C>A
ENST00000679512.1:c.794-222C>A	ENSP00000505113.1:n.794-222C>A
ENST00000679898.1:c.624-222C>A	ENSP00000505326.1:n.624-222C>A
ENST00000680288.1:c.747-222C>A	ENSP00000506001.1:n.747-222C>A
ENST00000680311.1:c.628-222C>A	ENSP00000505020.1:n.628-222C>A
ENST00000680471.1:c.*68-222C>A	ENSP00000506603.1:n.*68-222C>A
ENST00000680664.1:c.720-222C>A	ENSP00000506248.1:n.720-222C>A
ENST00000680931.1:c.*247-222C>A	ENSP00000504934.1:n.*247-222C>A
ENST00000681357.1:n.287-222C>A
ENST00000681444.1:c.897-222C>A	ENSP00000505359.1:n.897-222C>A
ENST00000368985.7:c.897-222C>A	ENSP00000357981.3:n.897-222C>A
ENST00000448301.6:c.747-222C>A	ENSP00000408414.1:n.747-222C>A
ENST00000472977.6:c.190-222C>A
ENST00000483930.1:c.445-222C>A	ENSP00000475812.1:n.445-222C>A
NM_001199739.1:c.747-222C>A	NP_001186668.1:n.747-222C>A
NM_004079.4:c.897-222C>A	NP_004070.3:n.897-222C>A
NM_004079.5:c.897-222C>A MANE Select	NP_004070.3:n.897-222C>A
NM_001199739.2:c.747-222C>A	NP_001186668.1:n.747-222C>A