Canonical Allele Identifier: CA2615475492

Gene: CTSC

Linked Data

• gnomAD v4: 11-88300439-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88300439A>G , CM000673.2:g.88300439A>G	GRCh38
NC_000011.9:g.88033607A>G , CM000673.1:g.88033607A>G	GRCh37
NC_000011.8:g.87673255A>G	NCBI36
NG_007952.1:g.42335T>C , LRG_50:g.42335T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.757+91T>C MANE Select	ENSP00000227266.4:n.757+91T>C
ENST00000527018.6:c.757+91T>C	ENSP00000432556.2:n.757+91T>C
ENST00000533897.2:n.896T>C
ENST00000676612.1:c.*564+91T>C	ENSP00000504440.1:n.*564+91T>C
ENST00000677208.1:c.*263+91T>C	ENSP00000504347.1:n.*263+91T>C
ENST00000677661.1:c.*434+91T>C	ENSP00000503323.1:n.*434+91T>C
ENST00000677802.1:c.*434+91T>C	ENSP00000504115.1:n.*434+91T>C
ENST00000678065.1:n.408T>C
ENST00000678395.1:c.*263+91T>C	ENSP00000503123.1:n.*263+91T>C
ENST00000678464.1:c.757+91T>C	ENSP00000503046.1:n.757+91T>C
ENST00000678506.1:c.718+91T>C	ENSP00000503580.1:n.718+91T>C
ENST00000678520.1:c.*408+91T>C	ENSP00000503361.1:n.*408+91T>C
ENST00000678554.1:c.757+91T>C	ENSP00000504541.1:n.757+91T>C
ENST00000678915.1:c.757+91T>C	ENSP00000504805.1:n.757+91T>C
ENST00000679224.1:c.394+91T>C	ENSP00000504475.1:n.394+91T>C
ENST00000227266.9:c.757+91T>C	ENSP00000227266.4:n.757+91T>C
ENST00000527018.5:c.627+91T>C
NM_001814.4:c.757+91T>C , LRG_50t1:c.757+91T>C	NP_001805.3:n.757+91T>C
NM_001814.5:c.757+91T>C	NP_001805.3:n.757+91T>C
NM_001814.6:c.757+91T>C MANE Select	NP_001805.4:n.757+91T>C