Canonical Allele Identifier: CA648963352
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415012dup , CM000666.2:g.73415012dup GRCh38
NC_000004.11:g.74280729dup , CM000666.1:g.74280729dup GRCh37
NC_000004.10:g.74499593dup NCBI36
NG_009291.1:g.15758dup

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1059-23dup MANE Select ENSP00000295897.4:n.1059-23dup
ENST00000295897.8:c.1059-23dup ENSP00000295897.4:n.1059-23dup
ENST00000401494.7:c.714-23dup ENSP00000384695.3:n.714-23dup
ENST00000415165.6:c.483-23dup ENSP00000401820.2:n.483-23dup
ENST00000476441.6:c.*338-23dup ENSP00000423727.1:n.*338-23dup
ENST00000484992.1:n.379-23dup
ENST00000503124.5:c.609-23dup ENSP00000421027.1:n.609-23dup
ENST00000504043.1:n.62-23dup
ENST00000505649.5:n.745-23dup
ENST00000509063.5:c.1059-23dup ENSP00000422784.1:n.1059-23dup
ENST00000511370.1:c.592-23dup
ENST00000621085.4:c.491-94dup ENSP00000483421.1:n.491-94dup
ENST00000621628.4:c.487-90dup ENSP00000480485.1:n.487-90dup
NM_000477.5:c.1059-23dup NP_000468.1:n.1059-23dup
NM_000477.6:c.1059-23dup NP_000468.1:n.1059-23dup
NM_000477.7:c.1059-23dup MANE Select NP_000468.1:n.1059-23dup