Canonical Allele Identifier: CA1146404317
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445794_15445820delinsCCCCTCACTCACCCATCCCCTCACTCA , CM000663.2:g.15445794_15445820delinsCCCCTCACTCACCCATCCCCTCACTCA GRCh38
NC_000001.10:g.15772289_15772315delinsCCCCTCACTCACCCATCCCCTCACTCA , CM000663.1:g.15772289_15772315delinsCCCCTCACTCACCCATCCCCTCACTCA GRCh37
NC_000001.9:g.15644876_15644902delinsCCCCTCACTCACCCATCCCCTCACTCA NCBI36
NG_009253.1:g.12352_12378delinsCCCCTCACTCACCCATCCCCTCACTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+45_792+71delinsCCCCTCACTCACCCATCCCCTCACTCA MANE Select ENSP00000365116.4:n.792+45_792+71delinsCCCCTCACTCACCCATCCCCTC...
ENST00000375943.6:c.*246+45_*246+71delinsCCCCTCACTCACCCATCCCCTCACTCA ENSP00000365110.2:n.*246+45_*246+71delinsCCCCTCACTCACCCATCCCC...
ENST00000375949.4:c.792+45_792+71delinsCCCCTCACTCACCCATCCCCTCACTCA ENSP00000365116.4:n.792+45_792+71delinsCCCCTCACTCACCCATCCCCTC...
ENST00000483406.1:n.556+45_556+71delinsCCCCTCACTCACCCATCCCCTCACTCA
NM_007272.2:c.792+45_792+71delinsCCCCTCACTCACCCATCCCCTCACTCA NP_009203.2:n.792+45_792+71delinsCCCCTCACTCACCCATCCCCTCACTCA
XM_011540550.1:c.646+45_646+71delinsCCCCTCACTCACCCATCCCCTCACTCA XP_011538852.1:n.646+45_646+71delinsCCCCTCACTCACCCATCCCCTCACT...
NM_007272.3:c.792+45_792+71delinsCCCCTCACTCACCCATCCCCTCACTCA MANE Select NP_009203.2:n.792+45_792+71delinsCCCCTCACTCACCCATCCCCTCACTCA