Canonical Allele Identifier: CA2647831691

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732998-G-T

Genomic Alleles

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

Transcript Alleles

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