Canonical Allele Identifier: CA2753572153
Gene: COL3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188996179_188996180insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC , CM000664.2:g.188996179_188996180insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC GRCh38
NC_000002.11:g.189860905_189860906insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC , CM000664.1:g.189860905_189860906insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC GRCh37
NC_000002.10:g.189569150_189569151insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC NCBI36
NG_007404.1:g.26807_26808insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC , LRG_3:g.26807_26808insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.1563+1_1563+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC ENSP00000415346.2:n.1563+1_1563+2insGAAGTCAAGGAGAAAGTGGTCGACC...
ENST00000304636.9:c.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC MANE Select ENSP00000304408.4:n.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACC...
ENST00000304636.7:c.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC ENSP00000304408.3:n.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACC...
ENST00000317840.9:c.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC ENSP00000315243.6:n.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACC...
NM_000090.3:c.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC , LRG_3t1:c.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC NP_000081.1:n.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCC...
NM_000090.4:c.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCCTCCTGGGCCATCTGGTCCCCGAGGTCAGCCTGGTGTCATGGGCTTCCCCGGTCC MANE Select NP_000081.2:n.1662+1_1662+2insGAAGTCAAGGAGAAAGTGGTCGACCAGGTCC...