Canonical Allele Identifier: CA382024943

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88042349T>G (hg19) ; chr11:g.88309181T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88309181T>G , CM000673.2:g.88309181T>G	GRCh38
NC_000011.9:g.88042349T>G , CM000673.1:g.88042349T>G	GRCh37
NC_000011.8:g.87681997T>G	NCBI36
NG_007952.1:g.33593A>C , LRG_50:g.33593A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.623A>C MANE Select	ENSP00000227266.4:p.His208Pro
ENST00000527018.6:c.623A>C	ENSP00000432556.2:p.His208Pro
ENST00000533897.2:n.671A>C
ENST00000676612.1:c.*430A>C	ENSP00000504440.1:n.*430A>C
ENST00000677208.1:c.*129A>C	ENSP00000504347.1:n.*129A>C
ENST00000677661.1:c.*300A>C	ENSP00000503323.1:n.*300A>C
ENST00000677802.1:c.*300A>C	ENSP00000504115.1:n.*300A>C
ENST00000678065.1:n.183A>C
ENST00000678395.1:c.*129A>C	ENSP00000503123.1:n.*129A>C
ENST00000678464.1:c.623A>C	ENSP00000503046.1:p.His208Pro
ENST00000678506.1:c.584A>C	ENSP00000503580.1:p.His195Pro
ENST00000678520.1:c.*292+3207A>C	ENSP00000503361.1:n.*292+3207A>C
ENST00000678554.1:c.623A>C	ENSP00000504541.1:p.His208Pro
ENST00000678915.1:c.623A>C	ENSP00000504805.1:p.His208Pro
ENST00000679224.1:c.260A>C	ENSP00000504475.1:p.His87Pro
ENST00000227266.9:c.623A>C	ENSP00000227266.4:p.His208Pro
ENST00000527018.5:c.493A>C
NM_001814.4:c.623A>C , LRG_50t1:c.623A>C	NP_001805.3:p.His208Pro
NM_001814.5:c.623A>C	NP_001805.3:p.His208Pro
NM_001814.6:c.623A>C MANE Select	NP_001805.4:p.His208Pro