Canonical Allele Identifier: CA1468143359
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415002C= , CM000666.2:g.73415002C= GRCh38
NC_000004.11:g.74280719C= , CM000666.1:g.74280719C= GRCh37
NC_000004.10:g.74499583C= NCBI36
NG_009291.1:g.15748C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1059-33C= MANE Select ENSP00000295897.4:n.1059-33C=
ENST00000295897.8:c.1059-33C= ENSP00000295897.4:n.1059-33C=
ENST00000401494.7:c.714-33C= ENSP00000384695.3:n.714-33C=
ENST00000415165.6:c.483-33C= ENSP00000401820.2:n.483-33C=
ENST00000476441.6:c.*338-33C= ENSP00000423727.1:n.*338-33C=
ENST00000484992.1:n.379-33C=
ENST00000503124.5:c.609-33C= ENSP00000421027.1:n.609-33C=
ENST00000504043.1:n.62-33C=
ENST00000505649.5:n.745-33C=
ENST00000509063.5:c.1059-33C= ENSP00000422784.1:n.1059-33C=
ENST00000511370.1:c.592-33C=
ENST00000621085.4:c.491-104C= ENSP00000483421.1:n.491-104C=
ENST00000621628.4:c.487-100C= ENSP00000480485.1:n.487-100C=
NM_000477.5:c.1059-33C= NP_000468.1:n.1059-33C=
NM_000477.6:c.1059-33C= NP_000468.1:n.1059-33C=
NM_000477.7:c.1059-33C= MANE Select NP_000468.1:n.1059-33C=