Canonical Allele Identifier: CA439798802
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406745dup , CM000666.2:g.73406745dup GRCh38
NC_000004.11:g.74272462dup , CM000666.1:g.74272462dup GRCh37
NC_000004.10:g.74491326dup NCBI36
NG_009291.1:g.7491dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.254dup MANE Select ENSP00000295897.4:p.Asn85LysfsTer3
ENST00000295897.8:c.254dup ENSP00000295897.4:p.Asn85LysfsTer3
ENST00000401494.7:c.137+1572dup ENSP00000384695.3:n.137+1572dup
ENST00000415165.6:c.137+1572dup ENSP00000401820.2:n.137+1572dup
ENST00000441319.5:c.260dup ENSP00000392541.1:p.Asn87LysfsTer3
ENST00000476441.6:c.79+2339dup ENSP00000423727.1:n.79+2339dup
ENST00000503124.5:c.16dup ENSP00000421027.1:p.Ile6AsnfsTer10
ENST00000509063.5:c.254dup ENSP00000422784.1:p.Asn85LysfsTer3
ENST00000510166.5:n.290dup
ENST00000514786.1:n.223dup
ENST00000515133.5:n.295dup
ENST00000621085.4:c.254dup ENSP00000483421.1:p.Asn85LysfsTer3
ENST00000621628.4:c.254dup ENSP00000480485.1:p.Asn85LysfsTer3
NM_000477.5:c.254dup NP_000468.1:p.Asn85LysfsTer3
NM_000477.6:c.254dup NP_000468.1:p.Asn85LysfsTer3
NM_000477.7:c.254dup MANE Select NP_000468.1:p.Asn85LysfsTer3