Canonical Allele Identifier: CA2647833893

Gene: CTSS

Linked Data

• gnomAD v4: 1-150754852-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150754852A>C , CM000663.2:g.150754852A>C	GRCh38
NC_000001.10:g.150727328A>C , CM000663.1:g.150727328A>C	GRCh37
NC_000001.9:g.148993952A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368985.8:c.399+149T>G MANE Select	ENSP00000357981.3:n.399+149T>G
ENST00000448301.7:c.399+149T>G	ENSP00000408414.2:n.399+149T>G
ENST00000472977.7:c.399+149T>G	ENSP00000475176.2:n.399+149T>G
ENST00000483930.2:c.399+149T>G	ENSP00000475812.2:n.399+149T>G
ENST00000607427.2:c.399+149T>G	ENSP00000475557.2:n.399+149T>G
ENST00000679512.1:c.399+149T>G	ENSP00000505113.1:n.399+149T>G
ENST00000679582.1:c.399+149T>G	ENSP00000504885.1:n.399+149T>G
ENST00000679898.1:c.127-2844T>G	ENSP00000505326.1:n.127-2844T>G
ENST00000680288.1:c.250-2844T>G	ENSP00000506001.1:n.250-2844T>G
ENST00000680311.1:c.399+149T>G	ENSP00000505020.1:n.399+149T>G
ENST00000680471.1:c.399+149T>G	ENSP00000506603.1:n.399+149T>G
ENST00000680664.1:c.222+149T>G	ENSP00000506248.1:n.222+149T>G
ENST00000680931.1:c.399+149T>G	ENSP00000504934.1:n.399+149T>G
ENST00000681444.1:c.399+149T>G	ENSP00000505359.1:n.399+149T>G
ENST00000681728.1:c.399+149T>G	ENSP00000505313.1:n.399+149T>G
ENST00000368985.7:c.399+149T>G	ENSP00000357981.3:n.399+149T>G
ENST00000448301.6:c.250-2844T>G	ENSP00000408414.1:n.250-2844T>G
ENST00000480760.1:n.338+149T>G
NM_001199739.1:c.250-2844T>G	NP_001186668.1:n.250-2844T>G
NM_004079.4:c.399+149T>G	NP_004070.3:n.399+149T>G
NM_004079.5:c.399+149T>G MANE Select	NP_004070.3:n.399+149T>G
NM_001199739.2:c.250-2844T>G	NP_001186668.1:n.250-2844T>G