Canonical Allele Identifier: CA2647831689

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732998-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732998G>A , CM000663.2:g.150732998G>A	GRCh38
NC_000001.10:g.150705474G>A , CM000663.1:g.150705474G>A	GRCh37
NC_000001.9:g.148972098G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*48C>T MANE Select	ENSP00000357981.3:n.*48C>T
ENST00000448301.7:c.*48C>T	ENSP00000408414.2:n.*48C>T
ENST00000472977.7:c.*48C>T	ENSP00000475176.2:n.*48C>T
ENST00000483930.2:c.*238C>T	ENSP00000475812.2:n.*238C>T
ENST00000607427.2:c.*48C>T	ENSP00000475557.2:n.*48C>T
ENST00000679512.1:c.*11C>T	ENSP00000505113.1:n.*11C>T
ENST00000679898.1:c.*48C>T	ENSP00000505326.1:n.*48C>T
ENST00000680288.1:c.*48C>T	ENSP00000506001.1:n.*48C>T
ENST00000680311.1:c.*127C>T	ENSP00000505020.1:n.*127C>T
ENST00000680471.1:c.*215C>T	ENSP00000506603.1:n.*215C>T
ENST00000680664.1:c.*48C>T	ENSP00000506248.1:n.*48C>T
ENST00000680931.1:c.*394C>T	ENSP00000504934.1:n.*394C>T
ENST00000681357.1:n.434C>T
ENST00000681444.1:c.*48C>T	ENSP00000505359.1:n.*48C>T
ENST00000368985.7:c.*48C>T	ENSP00000357981.3:n.*48C>T
ENST00000448301.6:c.*48C>T	ENSP00000408414.1:n.*48C>T
ENST00000472977.6:c.337C>T
ENST00000483930.1:c.592C>T	ENSP00000475812.1:n.592C>T
ENST00000607427.1:c.65C>T
NM_001199739.1:c.*48C>T	NP_001186668.1:n.*48C>T
NM_004079.4:c.*48C>T	NP_004070.3:n.*48C>T
NM_004079.5:c.*48C>T MANE Select	NP_004070.3:n.*48C>T
NM_001199739.2:c.*48C>T	NP_001186668.1:n.*48C>T