Canonical Allele Identifier: CA645517864
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418237del , CM000666.2:g.73418237del GRCh38
NC_000004.11:g.74283954del , CM000666.1:g.74283954del GRCh37
NC_000004.10:g.74502818del NCBI36
NG_009291.1:g.18983del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1578del MANE Select ENSP00000295897.4:p.Phe526LeufsTer?
ENST00000295897.8:c.1578del ENSP00000295897.4:p.Phe526LeufsTer?
ENST00000401494.7:c.1233del ENSP00000384695.3:p.Phe411LeufsTer?
ENST00000415165.6:c.1002del ENSP00000401820.2:p.Phe334LeufsTer?
ENST00000476441.6:c.*857del ENSP00000423727.1:n.*857del
ENST00000486939.1:n.232del
ENST00000503124.5:c.1128del ENSP00000421027.1:p.Phe376LeufsTer?
ENST00000505649.5:n.1125del
ENST00000509063.5:c.1578del ENSP00000422784.1:p.Phe526LeufsTer?
ENST00000511370.1:c.1111del
ENST00000621085.4:c.939del ENSP00000483421.1:p.Phe313LeufsTer?
ENST00000621628.4:c.939del ENSP00000480485.1:p.Phe313LeufsTer?
NM_000477.5:c.1578del NP_000468.1:p.Phe526LeufsTer?
NM_000477.6:c.1578del NP_000468.1:p.Phe526LeufsTer?
NM_000477.7:c.1578del MANE Select NP_000468.1:p.Phe526LeufsTer?