Canonical Allele Identifier: CA1468143355
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415000T= , CM000666.2:g.73415000T= GRCh38
NC_000004.11:g.74280717T= , CM000666.1:g.74280717T= GRCh37
NC_000004.10:g.74499581T= NCBI36
NG_009291.1:g.15746T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1059-35T= MANE Select ENSP00000295897.4:n.1059-35T=
ENST00000295897.8:c.1059-35T= ENSP00000295897.4:n.1059-35T=
ENST00000401494.7:c.714-35T= ENSP00000384695.3:n.714-35T=
ENST00000415165.6:c.483-35T= ENSP00000401820.2:n.483-35T=
ENST00000476441.6:c.*338-35T= ENSP00000423727.1:n.*338-35T=
ENST00000484992.1:n.379-35T=
ENST00000503124.5:c.609-35T= ENSP00000421027.1:n.609-35T=
ENST00000504043.1:n.62-35T=
ENST00000505649.5:n.745-35T=
ENST00000509063.5:c.1059-35T= ENSP00000422784.1:n.1059-35T=
ENST00000511370.1:c.592-35T=
ENST00000621085.4:c.491-106T= ENSP00000483421.1:n.491-106T=
ENST00000621628.4:c.487-102T= ENSP00000480485.1:n.487-102T=
NM_000477.5:c.1059-35T= NP_000468.1:n.1059-35T=
NM_000477.6:c.1059-35T= NP_000468.1:n.1059-35T=
NM_000477.7:c.1059-35T= MANE Select NP_000468.1:n.1059-35T=