Canonical Allele Identifier: CA1468148435
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718661929

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404316_73404317del , CM000666.2:g.73404316_73404317del GRCh38
NC_000004.11:g.74270033_74270034del , CM000666.1:g.74270033_74270034del GRCh37
NC_000004.10:g.74488897_74488898del NCBI36
NG_009291.1:g.5062_5063del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-12_-11del MANE Select ENSP00000295897.4:n.-12_-11del
ENST00000295897.8:c.-12_-11del ENSP00000295897.4:n.-12_-11del
ENST00000401494.7:c.-12_-11del ENSP00000384695.3:n.-12_-11del
ENST00000415165.6:c.-12_-11del ENSP00000401820.2:n.-12_-11del
ENST00000441319.5:n.48-53_48-52del ENSP00000392541.1:n.48-53_48-52del
ENST00000476441.6:c.-12_-11del ENSP00000423727.1:n.-12_-11del
ENST00000503124.5:c.-192_-191del ENSP00000421027.1:n.-192_-191del
ENST00000509063.5:c.-12_-11del ENSP00000422784.1:n.-12_-11del
ENST00000510166.5:n.30_31del
ENST00000514786.1:n.28_29del
ENST00000515133.5:n.30_31del
ENST00000621085.4:c.-12_-11del ENSP00000483421.1:n.-12_-11del
ENST00000621628.4:c.-12_-11del ENSP00000480485.1:n.-12_-11del
NM_000477.5:c.-12_-11del NP_000468.1:n.-12_-11del
NM_000477.6:c.-12_-11del NP_000468.1:n.-12_-11del
NM_000477.7:c.-12_-11del MANE Select NP_000468.1:n.-12_-11del