Canonical Allele Identifier: CA357237574
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73408798T>A , CM000666.2:g.73408798T>A GRCh38
NC_000004.11:g.74274515T>A , CM000666.1:g.74274515T>A GRCh37
NC_000004.10:g.74493379T>A NCBI36
NG_009291.1:g.9544T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.475T>A MANE Select ENSP00000295897.4:p.Leu159Met
ENST00000295897.8:c.475T>A ENSP00000295897.4:p.Leu159Met
ENST00000401494.7:c.138-557T>A ENSP00000384695.3:n.138-557T>A
ENST00000415165.6:c.138-3198T>A ENSP00000401820.2:n.138-3198T>A
ENST00000441319.5:c.481T>A ENSP00000392541.1:p.Leu161Met
ENST00000476441.6:c.80-557T>A ENSP00000423727.1:n.80-557T>A
ENST00000503124.5:c.33-557T>A ENSP00000421027.1:n.33-557T>A
ENST00000505649.5:n.161T>A
ENST00000509063.5:c.475T>A ENSP00000422784.1:p.Leu159Met
ENST00000510166.5:n.511T>A
ENST00000514786.1:n.444T>A
ENST00000515133.5:n.516T>A
ENST00000621085.4:c.475T>A ENSP00000483421.1:p.Leu159Met
ENST00000621628.4:c.475T>A ENSP00000480485.1:p.Leu159Met
NM_000477.5:c.475T>A NP_000468.1:p.Leu159Met
NM_000477.6:c.475T>A NP_000468.1:p.Leu159Met
NM_000477.7:c.475T>A MANE Select NP_000468.1:p.Leu159Met