Canonical Allele Identifier: CA476145200

Gene: CTSC

Linked Data

• MyVariant Identifiers: chr11:g.88027573G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.88294405G>A , CM000673.2:g.88294405G>A	GRCh38
NC_000011.9:g.88027573G>A , CM000673.1:g.88027573G>A	GRCh37
NC_000011.8:g.87667221G>A	NCBI36
NG_007952.1:g.48369C>T , LRG_50:g.48369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227266.10:c.993C>T MANE Select	ENSP00000227266.4:p.Cys331=
ENST00000533897.2:n.5306C>T
ENST00000676612.1:c.*800C>T	ENSP00000504440.1:n.*800C>T
ENST00000677208.1:c.*499C>T	ENSP00000504347.1:n.*499C>T
ENST00000677661.1:c.*670C>T	ENSP00000503323.1:n.*670C>T
ENST00000677802.1:c.*670C>T	ENSP00000504115.1:n.*670C>T
ENST00000678395.1:c.*499C>T	ENSP00000503123.1:n.*499C>T
ENST00000678464.1:c.960C>T	ENSP00000503046.1:p.Cys320=
ENST00000678506.1:c.954C>T	ENSP00000503580.1:p.Cys318=
ENST00000678520.1:c.*644C>T	ENSP00000503361.1:n.*644C>T
ENST00000678554.1:c.889+1728C>T	ENSP00000504541.1:n.889+1728C>T
ENST00000678915.1:c.861C>T	ENSP00000504805.1:p.Cys287=
ENST00000679224.1:c.630C>T	ENSP00000504475.1:p.Cys210=
ENST00000227266.9:c.993C>T	ENSP00000227266.4:p.Cys331=
ENST00000533897.1:n.3727C>T
NM_001814.4:c.993C>T , LRG_50t1:c.993C>T	NP_001805.3:p.Cys331=
NM_001814.5:c.993C>T	NP_001805.3:p.Cys331=
NM_001814.6:c.993C>T MANE Select	NP_001805.4:p.Cys331=