Canonical Allele Identifier: CA1155329095
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445917_15445989delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT , CM000663.2:g.15445917_15445989delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT GRCh38
NC_000001.10:g.15772412_15772484delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT , CM000663.1:g.15772412_15772484delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT GRCh37
NC_000001.9:g.15644999_15645071delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT NCBI36
NG_009253.1:g.12475_12547delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+168_792+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT MANE Select ENSP00000365116.4:n.792+168_792+240delinsGTCACTCATTCATGTATTTA...
ENST00000375943.6:c.*246+168_*246+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT ENSP00000365110.2:n.*246+168_*246+240delinsGTCACTCATTCATGTATT...
ENST00000375949.4:c.792+168_792+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT ENSP00000365116.4:n.792+168_792+240delinsGTCACTCATTCATGTATTTA...
ENST00000483406.1:n.556+168_556+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT
NM_007272.2:c.792+168_792+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT NP_009203.2:n.792+168_792+240delinsGTCACTCATTCATGTATTTATTCATT...
XM_011540550.1:c.646+168_646+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT XP_011538852.1:n.646+168_646+240delinsGTCACTCATTCATGTATTTATTC...
NM_007272.3:c.792+168_792+240delinsGTCACTCATTCATGTATTTATTCATTTATTCATTCACTCATGCATTCATTCATTCATTTATTCACTTATTCAT MANE Select NP_009203.2:n.792+168_792+240delinsGTCACTCATTCATGTATTTATTCATT...