Canonical Allele Identifier: CA2670936844
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.160dup MANE Select ENSP00000295897.4:p.Tyr54LeufsTer8
ENST00000295897.8:c.160dup ENSP00000295897.4:p.Tyr54LeufsTer8
ENST00000401494.7:c.137+1478dup ENSP00000384695.3:n.137+1478dup
ENST00000415165.6:c.137+1478dup ENSP00000401820.2:n.137+1478dup
ENST00000441319.5:c.166dup ENSP00000392541.1:p.Tyr56LeufsTer8
ENST00000476441.6:c.79+2245dup ENSP00000423727.1:n.79+2245dup
ENST00000503124.5:c.-79dup ENSP00000421027.1:n.-79dup
ENST00000509063.5:c.160dup ENSP00000422784.1:p.Tyr54LeufsTer8
ENST00000510166.5:n.196dup
ENST00000514786.1:n.129dup
ENST00000515133.5:n.201dup
ENST00000621085.4:c.160dup ENSP00000483421.1:p.Tyr54LeufsTer8
ENST00000621628.4:c.160dup ENSP00000480485.1:p.Tyr54LeufsTer8
NM_000477.5:c.160dup NP_000468.1:p.Tyr54LeufsTer8
NM_000477.6:c.160dup NP_000468.1:p.Tyr54LeufsTer8
NM_000477.7:c.160dup MANE Select NP_000468.1:p.Tyr54LeufsTer8