Canonical Allele Identifier: CA1155329124

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445939_15446003delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT , CM000663.2:g.15445939_15446003delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	GRCh38
NC_000001.10:g.15772434_15772498delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT , CM000663.1:g.15772434_15772498delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	GRCh37
NC_000001.9:g.15645021_15645085delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	NCBI36
NG_009253.1:g.12497_12561delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+190_792+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT MANE Select	ENSP00000365116.4:n.792+190_792+254delinsCATTTATTCATTCACTCATG...
ENST00000375943.6:c.*246+190_*246+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	ENSP00000365110.2:n.*246+190_*246+254delinsCATTTATTCATTCACTCA...
ENST00000375949.4:c.792+190_792+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	ENSP00000365116.4:n.792+190_792+254delinsCATTTATTCATTCACTCATG...
ENST00000483406.1:n.556+190_556+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT
NM_007272.2:c.792+190_792+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	NP_009203.2:n.792+190_792+254delinsCATTTATTCATTCACTCATGCATTCA...
XM_011540550.1:c.646+190_646+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT	XP_011538852.1:n.646+190_646+254delinsCATTTATTCATTCACTCATGCAT...
NM_007272.3:c.792+190_792+254delinsCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCATTCACTCATTCATGT MANE Select	NP_009203.2:n.792+190_792+254delinsCATTTATTCATTCACTCATGCATTCA...