Canonical Allele Identifier: CA2647831681

Gene: CTSS

Linked Data

• gnomAD v4: 1-150732972-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732972G>T , CM000663.2:g.150732972G>T	GRCh38
NC_000001.10:g.150705448G>T , CM000663.1:g.150705448G>T	GRCh37
NC_000001.9:g.148972072G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*74C>A MANE Select	ENSP00000357981.3:n.*74C>A
ENST00000448301.7:c.*74C>A	ENSP00000408414.2:n.*74C>A
ENST00000472977.7:c.*74C>A	ENSP00000475176.2:n.*74C>A
ENST00000483930.2:c.*264C>A	ENSP00000475812.2:n.*264C>A
ENST00000607427.2:c.*74C>A	ENSP00000475557.2:n.*74C>A
ENST00000679512.1:c.*37C>A	ENSP00000505113.1:n.*37C>A
ENST00000679898.1:c.*74C>A	ENSP00000505326.1:n.*74C>A
ENST00000680288.1:c.*74C>A	ENSP00000506001.1:n.*74C>A
ENST00000680311.1:c.*153C>A	ENSP00000505020.1:n.*153C>A
ENST00000680471.1:c.*241C>A	ENSP00000506603.1:n.*241C>A
ENST00000680664.1:c.*74C>A	ENSP00000506248.1:n.*74C>A
ENST00000680931.1:c.*420C>A	ENSP00000504934.1:n.*420C>A
ENST00000681357.1:n.460C>A
ENST00000681444.1:c.*74C>A	ENSP00000505359.1:n.*74C>A
ENST00000368985.7:c.*74C>A	ENSP00000357981.3:n.*74C>A
ENST00000448301.6:c.*74C>A	ENSP00000408414.1:n.*74C>A
ENST00000472977.6:c.363C>A
ENST00000483930.1:c.618C>A	ENSP00000475812.1:n.618C>A
ENST00000607427.1:c.91C>A
NM_001199739.1:c.*74C>A	NP_001186668.1:n.*74C>A
NM_004079.4:c.*74C>A	NP_004070.3:n.*74C>A
NM_004079.5:c.*74C>A MANE Select	NP_004070.3:n.*74C>A
NM_001199739.2:c.*74C>A	NP_001186668.1:n.*74C>A