Canonical Allele Identifier: CA2558422989
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406728_73406729insACGCTAGAGAACAAATCATGTATGGGTATAG , CM000666.2:g.73406728_73406729insACGCTAGAGAACAAATCATGTATGGGTATAG GRCh38
NC_000004.11:g.74272445_74272446insACGCTAGAGAACAAATCATGTATGGGTATAG , CM000666.1:g.74272445_74272446insACGCTAGAGAACAAATCATGTATGGGTATAG GRCh37
NC_000004.10:g.74491309_74491310insACGCTAGAGAACAAATCATGTATGGGTATAG NCBI36
NG_009291.1:g.7474_7475insACGCTAGAGAACAAATCATGTATGGGTATAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG MANE Select ENSP00000295897.4:p.Asp80ThrfsTer12
ENST00000295897.8:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000295897.4:p.Asp80ThrfsTer12
ENST00000401494.7:c.137+1555_137+1556insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000384695.3:n.137+1555_137+1556insACGCTAGAGAACAAATCATGT...
ENST00000415165.6:c.137+1555_137+1556insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000401820.2:n.137+1555_137+1556insACGCTAGAGAACAAATCATGT...
ENST00000441319.5:c.243_244insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000392541.1:p.Asp82ThrfsTer12
ENST00000476441.6:c.79+2322_79+2323insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000423727.1:n.79+2322_79+2323insACGCTAGAGAACAAATCATGTAT...
ENST00000503124.5:c.-2_-1insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000421027.1:n.-2_-1insACGCTAGAGAACAAATCATGTATGGGTATAG
ENST00000509063.5:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000422784.1:p.Asp80ThrfsTer12
ENST00000510166.5:n.273_274insACGCTAGAGAACAAATCATGTATGGGTATAG
ENST00000514786.1:n.206_207insACGCTAGAGAACAAATCATGTATGGGTATAG
ENST00000515133.5:n.278_279insACGCTAGAGAACAAATCATGTATGGGTATAG
ENST00000621085.4:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000483421.1:p.Asp80ThrfsTer12
ENST00000621628.4:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG ENSP00000480485.1:p.Asp80ThrfsTer12
NM_000477.5:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG NP_000468.1:p.Asp80ThrfsTer12
NM_000477.6:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG NP_000468.1:p.Asp80ThrfsTer12
NM_000477.7:c.237_238insACGCTAGAGAACAAATCATGTATGGGTATAG MANE Select NP_000468.1:p.Asp80ThrfsTer12