Canonical Allele Identifier: CA889263877

Gene: CTSS

Linked Data

• dbSNP Id: rs1181497409
• MyVariant Identifiers: chr1:g.150705428A>G (hg19) ; chr1:g.150732952A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732952A>G , CM000663.2:g.150732952A>G	GRCh38
NC_000001.10:g.150705428A>G , CM000663.1:g.150705428A>G	GRCh37
NC_000001.9:g.148972052A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*94T>C MANE Select	ENSP00000357981.3:n.*94T>C
ENST00000448301.7:c.*94T>C	ENSP00000408414.2:n.*94T>C
ENST00000472977.7:c.*94T>C	ENSP00000475176.2:n.*94T>C
ENST00000483930.2:c.*284T>C	ENSP00000475812.2:n.*284T>C
ENST00000607427.2:c.*94T>C	ENSP00000475557.2:n.*94T>C
ENST00000679512.1:c.*57T>C	ENSP00000505113.1:n.*57T>C
ENST00000679898.1:c.*94T>C	ENSP00000505326.1:n.*94T>C
ENST00000680288.1:c.*94T>C	ENSP00000506001.1:n.*94T>C
ENST00000680311.1:c.*173T>C	ENSP00000505020.1:n.*173T>C
ENST00000680471.1:c.*261T>C	ENSP00000506603.1:n.*261T>C
ENST00000680664.1:c.*94T>C	ENSP00000506248.1:n.*94T>C
ENST00000680931.1:c.*440T>C	ENSP00000504934.1:n.*440T>C
ENST00000681357.1:n.480T>C
ENST00000681444.1:c.*94T>C	ENSP00000505359.1:n.*94T>C
ENST00000368985.7:c.*94T>C	ENSP00000357981.3:n.*94T>C
ENST00000448301.6:c.*94T>C	ENSP00000408414.1:n.*94T>C
ENST00000472977.6:c.383T>C
ENST00000483930.1:c.638T>C	ENSP00000475812.1:n.638T>C
ENST00000607427.1:c.111T>C
NM_001199739.1:c.*94T>C	NP_001186668.1:n.*94T>C
NM_004079.4:c.*94T>C	NP_004070.3:n.*94T>C
NM_004079.5:c.*94T>C MANE Select	NP_004070.3:n.*94T>C
NM_001199739.2:c.*94T>C	NP_001186668.1:n.*94T>C