Canonical Allele Identifier: CA8120473
Gene: CTRL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67931196C>T , CM000678.2:g.67931196C>T GRCh38
NC_000016.9:g.67965099C>T , CM000678.1:g.67965099C>T GRCh37
NC_000016.8:g.66522600C>T NCBI36
NG_051639.1:g.5680G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000574481.6:c.58G>A MANE Select ENSP00000458537.2:p.Gly20Ser
ENST00000571044.5:c.58G>A ENSP00000461842.1:p.Gly20Ser
ENST00000571605.1:c.53-197G>A ENSP00000458598.1:n.53-197G>A
ENST00000572144.5:n.1170G>A
ENST00000573493.1:c.499-197G>A
ENST00000574481.5:c.58G>A ENSP00000458537.2:p.Gly20Ser
ENST00000575231.1:n.4329G>A
ENST00000575302.1:n.479G>A
ENST00000576408.1:n.314-197G>A
ENST00000576915.1:n.290G>A
NM_001907.2:c.58G>A NP_001898.1:p.Gly20Ser
NM_001907.3:c.58G>A MANE Select NP_001898.1:p.Gly20Ser