Canonical Allele Identifier: CA1989482751

Gene: CTSC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294350_88294351delinsCT , CM000673.2:g.88294350_88294351delinsCT	GRCh38
NC_000011.9:g.88027518_88027519delinsCT , CM000673.1:g.88027518_88027519delinsCT	GRCh37
NC_000011.8:g.87667166_87667167delinsCT	NCBI36
NG_007952.1:g.48423_48424delinsAG , LRG_50:g.48423_48424delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000227266.10:c.1047_1048delinsAG MANE Select	ENSP00000227266.4:p.Gly349=
ENST00000533897.2:n.5360_5361delinsAG
ENST00000676612.1:c.*854_*855delinsAG	ENSP00000504440.1:n.*854_*855delinsAG
ENST00000677208.1:c.*553_*554delinsAG	ENSP00000504347.1:n.*553_*554delinsAG
ENST00000677661.1:c.*724_*725delinsAG	ENSP00000503323.1:n.*724_*725delinsAG
ENST00000677802.1:c.*724_*725delinsAG	ENSP00000504115.1:n.*724_*725delinsAG
ENST00000678395.1:c.*553_*554delinsAG	ENSP00000503123.1:n.*553_*554delinsAG
ENST00000678464.1:c.1014_1015delinsAG	ENSP00000503046.1:p.Gly338=
ENST00000678506.1:c.1008_1009delinsAG	ENSP00000503580.1:p.Gly336=
ENST00000678520.1:c.*698_*699delinsAG	ENSP00000503361.1:n.*698_*699delinsAG
ENST00000678554.1:c.889+1782_889+1783delinsAG	ENSP00000504541.1:n.889+1782_889+1783deli...
ENST00000678915.1:c.915_916delinsAG	ENSP00000504805.1:p.Gly305=
ENST00000679224.1:c.684_685delinsAG	ENSP00000504475.1:p.Gly228=
ENST00000227266.9:c.1047_1048delinsAG	ENSP00000227266.4:p.Gly349=
ENST00000533897.1:n.3781_3782delinsAG
NM_001814.4:c.1047_1048delinsAG , LRG_50t1:c.1047_1048delinsAG	NP_001805.3:p.Gly349=
NM_001814.5:c.1047_1048delinsAG	NP_001805.3:p.Gly349=
NM_001814.6:c.1047_1048delinsAG MANE Select	NP_001805.4:p.Gly349=