Canonical Allele Identifier: CA1155329140

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445953_15445969delinsCTCATGCATTCATTCAT , CM000663.2:g.15445953_15445969delinsCTCATGCATTCATTCAT	GRCh38
NC_000001.10:g.15772448_15772464delinsCTCATGCATTCATTCAT , CM000663.1:g.15772448_15772464delinsCTCATGCATTCATTCAT	GRCh37
NC_000001.9:g.15645035_15645051delinsCTCATGCATTCATTCAT	NCBI36
NG_009253.1:g.12511_12527delinsCTCATGCATTCATTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+204_792+220delinsCTCATGCATTCATTCAT MANE Select	ENSP00000365116.4:n.792+204_792+220delinsCTCATGCATTCATTCAT
ENST00000375943.6:c.*246+204_*246+220delinsCTCATGCATTCATTCAT	ENSP00000365110.2:n.*246+204_*246+220delinsCTCATGCATTCATTCAT
ENST00000375949.4:c.792+204_792+220delinsCTCATGCATTCATTCAT	ENSP00000365116.4:n.792+204_792+220delinsCTCATGCATTCATTCAT
ENST00000483406.1:n.556+204_556+220delinsCTCATGCATTCATTCAT
NM_007272.2:c.792+204_792+220delinsCTCATGCATTCATTCAT	NP_009203.2:n.792+204_792+220delinsCTCATGCATTCATTCAT
XM_011540550.1:c.646+204_646+220delinsCTCATGCATTCATTCAT	XP_011538852.1:n.646+204_646+220delinsCTCATGCATTCATTCAT
NM_007272.3:c.792+204_792+220delinsCTCATGCATTCATTCAT MANE Select	NP_009203.2:n.792+204_792+220delinsCTCATGCATTCATTCAT