Canonical Allele Identifier: CA1468151049
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406809_73406819delinsCCCAAGCATTT , CM000666.2:g.73406809_73406819delinsCCCAAGCATTT GRCh38
NC_000004.11:g.74272526_74272536delinsCCCAAGCATTT , CM000666.1:g.74272526_74272536delinsCCCAAGCATTT GRCh37
NC_000004.10:g.74491390_74491400delinsCCCAAGCATTT NCBI36
NG_009291.1:g.7555_7565delinsCCCAAGCATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.270+48_270+58delinsCCCAAGCATTT MANE Select ENSP00000295897.4:n.270+48_270+58delinsCCCAAGCATTT
ENST00000295897.8:c.270+48_270+58delinsCCCAAGCATTT ENSP00000295897.4:n.270+48_270+58delinsCCCAAGCATTT
ENST00000401494.7:c.137+1636_137+1646delinsCCCAAGCATTT ENSP00000384695.3:n.137+1636_137+1646delinsCCCAAGCATTT
ENST00000415165.6:c.137+1636_137+1646delinsCCCAAGCATTT ENSP00000401820.2:n.137+1636_137+1646delinsCCCAAGCATTT
ENST00000441319.5:c.276+48_276+58delinsCCCAAGCATTT ENSP00000392541.1:n.276+48_276+58delinsCCCAAGCATTT
ENST00000476441.6:c.79+2403_79+2413delinsCCCAAGCATTT ENSP00000423727.1:n.79+2403_79+2413delinsCCCAAGCATTT
ENST00000503124.5:c.32+48_32+58delinsCCCAAGCATTT ENSP00000421027.1:n.32+48_32+58delinsCCCAAGCATTT
ENST00000509063.5:c.270+48_270+58delinsCCCAAGCATTT ENSP00000422784.1:n.270+48_270+58delinsCCCAAGCATTT
ENST00000510166.5:n.306+48_306+58delinsCCCAAGCATTT
ENST00000514786.1:n.239+48_239+58delinsCCCAAGCATTT
ENST00000515133.5:n.311+48_311+58delinsCCCAAGCATTT
ENST00000621085.4:c.270+48_270+58delinsCCCAAGCATTT ENSP00000483421.1:n.270+48_270+58delinsCCCAAGCATTT
ENST00000621628.4:c.270+48_270+58delinsCCCAAGCATTT ENSP00000480485.1:n.270+48_270+58delinsCCCAAGCATTT
NM_000477.5:c.270+48_270+58delinsCCCAAGCATTT NP_000468.1:n.270+48_270+58delinsCCCAAGCATTT
NM_000477.6:c.270+48_270+58delinsCCCAAGCATTT NP_000468.1:n.270+48_270+58delinsCCCAAGCATTT
NM_000477.7:c.270+48_270+58delinsCCCAAGCATTT MANE Select NP_000468.1:n.270+48_270+58delinsCCCAAGCATTT