Canonical Allele Identifier: CA382022193

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027608C>A (hg19) ; chr11:g.88294440C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294440C>A , CM000673.2:g.88294440C>A	GRCh38
NC_000011.9:g.88027608C>A , CM000673.1:g.88027608C>A	GRCh37
NC_000011.8:g.87667256C>A	NCBI36
NG_007952.1:g.48334G>T , LRG_50:g.48334G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.958G>T MANE Select	ENSP00000227266.4:p.Ala320Ser
ENST00000533897.2:n.5271G>T
ENST00000676612.1:c.*765G>T	ENSP00000504440.1:n.*765G>T
ENST00000677208.1:c.*464G>T	ENSP00000504347.1:n.*464G>T
ENST00000677661.1:c.*635G>T	ENSP00000503323.1:n.*635G>T
ENST00000677802.1:c.*635G>T	ENSP00000504115.1:n.*635G>T
ENST00000678395.1:c.*464G>T	ENSP00000503123.1:n.*464G>T
ENST00000678464.1:c.925G>T	ENSP00000503046.1:p.Ala309Ser
ENST00000678506.1:c.919G>T	ENSP00000503580.1:p.Ala307Ser
ENST00000678520.1:c.*609G>T	ENSP00000503361.1:n.*609G>T
ENST00000678554.1:c.889+1693G>T	ENSP00000504541.1:n.889+1693G>T
ENST00000678915.1:c.826G>T	ENSP00000504805.1:p.Ala276Ser
ENST00000679224.1:c.595G>T	ENSP00000504475.1:p.Ala199Ser
ENST00000227266.9:c.958G>T	ENSP00000227266.4:p.Ala320Ser
ENST00000533897.1:n.3692G>T
NM_001814.4:c.958G>T , LRG_50t1:c.958G>T	NP_001805.3:p.Ala320Ser
NM_001814.5:c.958G>T	NP_001805.3:p.Ala320Ser
NM_001814.6:c.958G>T MANE Select	NP_001805.4:p.Ala320Ser