Canonical Allele Identifier: CA2615475545

Gene: CTSC

Linked Data

• gnomAD v4: 11-88300502-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88300502A>G , CM000673.2:g.88300502A>G	GRCh38
NC_000011.9:g.88033670A>G , CM000673.1:g.88033670A>G	GRCh37
NC_000011.8:g.87673318A>G	NCBI36
NG_007952.1:g.42272T>C , LRG_50:g.42272T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.757+28T>C MANE Select	ENSP00000227266.4:n.757+28T>C
ENST00000527018.6:c.757+28T>C	ENSP00000432556.2:n.757+28T>C
ENST00000533897.2:n.833T>C
ENST00000676612.1:c.*564+28T>C	ENSP00000504440.1:n.*564+28T>C
ENST00000677208.1:c.*263+28T>C	ENSP00000504347.1:n.*263+28T>C
ENST00000677661.1:c.*434+28T>C	ENSP00000503323.1:n.*434+28T>C
ENST00000677802.1:c.*434+28T>C	ENSP00000504115.1:n.*434+28T>C
ENST00000678065.1:n.345T>C
ENST00000678395.1:c.*263+28T>C	ENSP00000503123.1:n.*263+28T>C
ENST00000678464.1:c.757+28T>C	ENSP00000503046.1:n.757+28T>C
ENST00000678506.1:c.718+28T>C	ENSP00000503580.1:n.718+28T>C
ENST00000678520.1:c.*408+28T>C	ENSP00000503361.1:n.*408+28T>C
ENST00000678554.1:c.757+28T>C	ENSP00000504541.1:n.757+28T>C
ENST00000678915.1:c.757+28T>C	ENSP00000504805.1:n.757+28T>C
ENST00000679224.1:c.394+28T>C	ENSP00000504475.1:n.394+28T>C
ENST00000227266.9:c.757+28T>C	ENSP00000227266.4:n.757+28T>C
ENST00000527018.5:c.627+28T>C
NM_001814.4:c.757+28T>C , LRG_50t1:c.757+28T>C	NP_001805.3:n.757+28T>C
NM_001814.5:c.757+28T>C	NP_001805.3:n.757+28T>C
NM_001814.6:c.757+28T>C MANE Select	NP_001805.4:n.757+28T>C