Canonical Allele Identifier: CA127950
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18224
ClinVar RCV Id: RCV000019885
dbSNP Id: rs77449454

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73413448dup , CM000666.2:g.73413448dup GRCh38
NC_000004.11:g.74279165dup , CM000666.1:g.74279165dup GRCh37
NC_000004.10:g.74498029dup NCBI36
NG_009291.1:g.14194dup

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.872dup MANE Select ENSP00000295897.4:p.Asn291LysfsTer8
ENST00000295897.8:c.872dup ENSP00000295897.4:p.Asn291LysfsTer8
ENST00000401494.7:c.527dup ENSP00000384695.3:p.Asn176LysfsTer8
ENST00000415165.6:c.296dup ENSP00000401820.2:p.Asn99LysfsTer8
ENST00000476441.6:c.*151dup ENSP00000423727.1:n.*151dup
ENST00000484992.1:n.192dup
ENST00000503124.5:c.422dup ENSP00000421027.1:p.Asn141LysfsTer8
ENST00000505649.5:n.558dup
ENST00000509063.5:c.872dup ENSP00000422784.1:p.Asn291LysfsTer8
ENST00000511370.1:n.405dup
ENST00000621085.4:c.491-1658dup ENSP00000483421.1:n.491-1658dup
ENST00000621628.4:c.487-1654dup ENSP00000480485.1:n.487-1654dup
NM_000477.5:c.872dup NP_000468.1:p.Asn291LysfsTer8
NM_000477.6:c.872dup NP_000468.1:p.Asn291LysfsTer8
NM_000477.7:c.872dup MANE Select NP_000468.1:p.Asn291LysfsTer8