Canonical Allele Identifier: CA2479286209

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733153_150733157delinsAAAAG , CM000663.2:g.150733153_150733157delinsAAAAG	GRCh38
NC_000001.10:g.150705629_150705633delinsAAAAG , CM000663.1:g.150705629_150705633delinsAAAAG	GRCh37
NC_000001.9:g.148972253_148972257delinsAAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897-12_897-8delinsCTTTT MANE Select	ENSP00000357981.3:n.897-12_897-8delinsCTTTT
ENST00000448301.7:c.669-12_669-8delinsCTTTT	ENSP00000408414.2:n.669-12_669-8delinsCTTTT
ENST00000472977.7:c.897-12_897-8delinsCTTTT	ENSP00000475176.2:n.897-12_897-8delinsCTTTT
ENST00000483930.2:c.*91-12_*91-8delinsCTTTT	ENSP00000475812.2:n.*91-12_*91-8delinsCTTTT
ENST00000607427.2:c.897-12_897-8delinsCTTTT	ENSP00000475557.2:n.897-12_897-8delinsCTTTT
ENST00000679512.1:c.794-12_794-8delinsCTTTT	ENSP00000505113.1:n.794-12_794-8delinsCTTTT
ENST00000679898.1:c.624-12_624-8delinsCTTTT	ENSP00000505326.1:n.624-12_624-8delinsCTTTT
ENST00000680288.1:c.747-12_747-8delinsCTTTT	ENSP00000506001.1:n.747-12_747-8delinsCTTTT
ENST00000680311.1:c.628-12_628-8delinsCTTTT	ENSP00000505020.1:n.628-12_628-8delinsCTTTT
ENST00000680471.1:c.*68-12_*68-8delinsCTTTT	ENSP00000506603.1:n.*68-12_*68-8delinsCTTTT
ENST00000680664.1:c.720-12_720-8delinsCTTTT	ENSP00000506248.1:n.720-12_720-8delinsCTTTT
ENST00000680931.1:c.*247-12_*247-8delinsCTTTT	ENSP00000504934.1:n.*247-12_*247-8delinsCTTTT
ENST00000681357.1:n.287-12_287-8delinsCTTTT
ENST00000681444.1:c.897-12_897-8delinsCTTTT	ENSP00000505359.1:n.897-12_897-8delinsCTTTT
ENST00000368985.7:c.897-12_897-8delinsCTTTT	ENSP00000357981.3:n.897-12_897-8delinsCTTTT
ENST00000448301.6:c.747-12_747-8delinsCTTTT	ENSP00000408414.1:n.747-12_747-8delinsCTTTT
ENST00000472977.6:c.190-12_190-8delinsCTTTT
ENST00000483930.1:c.445-12_445-8delinsCTTTT	ENSP00000475812.1:n.445-12_445-8delinsCTTTT
NM_001199739.1:c.747-12_747-8delinsCTTTT	NP_001186668.1:n.747-12_747-8delinsCTTTT
NM_004079.4:c.897-12_897-8delinsCTTTT	NP_004070.3:n.897-12_897-8delinsCTTTT
NM_004079.5:c.897-12_897-8delinsCTTTT MANE Select	NP_004070.3:n.897-12_897-8delinsCTTTT
NM_001199739.2:c.747-12_747-8delinsCTTTT	NP_001186668.1:n.747-12_747-8delinsCTTTT