Canonical Allele Identifier: CA1468148103
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73419519G= , CM000666.2:g.73419519G= GRCh38
NC_000004.11:g.74285236G= , CM000666.1:g.74285236G= GRCh37
NC_000004.10:g.74504100G= NCBI36
NG_009291.1:g.20265G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1665G= MANE Select ENSP00000295897.4:p.Glu555=
ENST00000295897.8:c.1665G= ENSP00000295897.4:p.Glu555=
ENST00000401494.7:c.1320G= ENSP00000384695.3:p.Glu440=
ENST00000415165.6:c.1089G= ENSP00000401820.2:p.Glu363=
ENST00000476441.6:c.*944G= ENSP00000423727.1:n.*944G=
ENST00000486939.1:n.319G=
ENST00000503124.5:c.1215G= ENSP00000421027.1:p.Glu405=
ENST00000505649.5:n.1212G=
ENST00000508932.5:n.175+64G=
ENST00000509063.5:c.1665G= ENSP00000422784.1:p.Glu555=
ENST00000511370.1:c.1198G=
ENST00000621085.4:c.1026G= ENSP00000483421.1:p.Glu342=
ENST00000621628.4:c.1026G= ENSP00000480485.1:p.Glu342=
NM_000477.5:c.1665G= NP_000468.1:p.Glu555=
NM_000477.6:c.1665G= NP_000468.1:p.Glu555=
NM_000477.7:c.1665G= MANE Select NP_000468.1:p.Glu555=