Canonical Allele Identifier: CA1468143311
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73414970T= , CM000666.2:g.73414970T= GRCh38
NC_000004.11:g.74280687T= , CM000666.1:g.74280687T= GRCh37
NC_000004.10:g.74499551T= NCBI36
NG_009291.1:g.15716T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1059-65T= MANE Select ENSP00000295897.4:n.1059-65T=
ENST00000295897.8:c.1059-65T= ENSP00000295897.4:n.1059-65T=
ENST00000401494.7:c.714-65T= ENSP00000384695.3:n.714-65T=
ENST00000415165.6:c.483-65T= ENSP00000401820.2:n.483-65T=
ENST00000476441.6:c.*338-65T= ENSP00000423727.1:n.*338-65T=
ENST00000484992.1:n.379-65T=
ENST00000503124.5:c.609-65T= ENSP00000421027.1:n.609-65T=
ENST00000504043.1:n.62-65T=
ENST00000505649.5:n.745-65T=
ENST00000509063.5:c.1059-65T= ENSP00000422784.1:n.1059-65T=
ENST00000511370.1:c.592-65T=
ENST00000621085.4:c.491-136T= ENSP00000483421.1:n.491-136T=
ENST00000621628.4:c.487-132T= ENSP00000480485.1:n.487-132T=
NM_000477.5:c.1059-65T= NP_000468.1:n.1059-65T=
NM_000477.6:c.1059-65T= NP_000468.1:n.1059-65T=
NM_000477.7:c.1059-65T= MANE Select NP_000468.1:n.1059-65T=