Canonical Allele Identifier: CA1468150861
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406651T= , CM000666.2:g.73406651T= GRCh38
NC_000004.11:g.74272368T= , CM000666.1:g.74272368T= GRCh37
NC_000004.10:g.74491232T= NCBI36
NG_009291.1:g.7397T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.160T= MANE Select ENSP00000295897.4:p.Tyr54=
ENST00000295897.8:c.160T= ENSP00000295897.4:p.Tyr54=
ENST00000401494.7:c.137+1478T= ENSP00000384695.3:n.137+1478T=
ENST00000415165.6:c.137+1478T= ENSP00000401820.2:n.137+1478T=
ENST00000441319.5:c.166T= ENSP00000392541.1:p.Tyr56=
ENST00000476441.6:c.79+2245T= ENSP00000423727.1:n.79+2245T=
ENST00000503124.5:c.-79T= ENSP00000421027.1:n.-79T=
ENST00000509063.5:c.160T= ENSP00000422784.1:p.Tyr54=
ENST00000510166.5:n.196T=
ENST00000514786.1:n.129T=
ENST00000515133.5:n.201T=
ENST00000621085.4:c.160T= ENSP00000483421.1:p.Tyr54=
ENST00000621628.4:c.160T= ENSP00000480485.1:p.Tyr54=
NM_000477.5:c.160T= NP_000468.1:p.Tyr54=
NM_000477.6:c.160T= NP_000468.1:p.Tyr54=
NM_000477.7:c.160T= MANE Select NP_000468.1:p.Tyr54=