Canonical Allele Identifier: CA1468151105
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406866_73406867delinsAT , CM000666.2:g.73406866_73406867delinsAT GRCh38
NC_000004.11:g.74272583_74272584delinsAT , CM000666.1:g.74272583_74272584delinsAT GRCh37
NC_000004.10:g.74491447_74491448delinsAT NCBI36
NG_009291.1:g.7612_7613delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.270+105_270+106delinsAT MANE Select ENSP00000295897.4:n.270+105_270+106delinsAT
ENST00000295897.8:c.270+105_270+106delinsAT ENSP00000295897.4:n.270+105_270+106delinsAT
ENST00000401494.7:c.137+1693_137+1694delinsAT ENSP00000384695.3:n.137+1693_137+1694delinsAT
ENST00000415165.6:c.137+1693_137+1694delinsAT ENSP00000401820.2:n.137+1693_137+1694delinsAT
ENST00000441319.5:c.276+105_276+106delinsAT ENSP00000392541.1:n.276+105_276+106delinsAT
ENST00000476441.6:c.79+2460_79+2461delinsAT ENSP00000423727.1:n.79+2460_79+2461delinsAT
ENST00000503124.5:c.32+105_32+106delinsAT ENSP00000421027.1:n.32+105_32+106delinsAT
ENST00000509063.5:c.270+105_270+106delinsAT ENSP00000422784.1:n.270+105_270+106delinsAT
ENST00000510166.5:n.306+105_306+106delinsAT
ENST00000514786.1:n.239+105_239+106delinsAT
ENST00000515133.5:n.311+105_311+106delinsAT
ENST00000621085.4:c.270+105_270+106delinsAT ENSP00000483421.1:n.270+105_270+106delinsAT
ENST00000621628.4:c.270+105_270+106delinsAT ENSP00000480485.1:n.270+105_270+106delinsAT
NM_000477.5:c.270+105_270+106delinsAT NP_000468.1:n.270+105_270+106delinsAT
NM_000477.6:c.270+105_270+106delinsAT NP_000468.1:n.270+105_270+106delinsAT
NM_000477.7:c.270+105_270+106delinsAT MANE Select NP_000468.1:n.270+105_270+106delinsAT