Canonical Allele Identifier: CA2670966781
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420322del , CM000666.2:g.73420322del GRCh38
NC_000004.11:g.74286039del , CM000666.1:g.74286039del GRCh37
NC_000004.10:g.74504903del NCBI36
NG_009291.1:g.21068del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.*23+1del
ENST00000295897.8:c.*23+1del
ENST00000401494.7:c.*23+1del
ENST00000415165.6:c.*23+1del
ENST00000476441.6:c.*1132+1del
ENST00000495173.1:n.161+1del
ENST00000503124.5:c.*23+1del
ENST00000505649.5:n.1400+1del
ENST00000508932.5:n.243+1del
ENST00000509063.5:c.1785+683del ENSP00000422784.1:n.1785+683del
ENST00000511370.1:c.1386+1del
ENST00000621085.4:c.*23+1del
ENST00000621628.4:c.*23+1del
NM_000477.5:c.*23+1del
NM_000477.6:c.*23+1del
NM_000477.7:c.*23+1del