Canonical Allele Identifier: CA1468143548
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415115C= , CM000666.2:g.73415115C= GRCh38
NC_000004.11:g.74280832C= , CM000666.1:g.74280832C= GRCh37
NC_000004.10:g.74499696C= NCBI36
NG_009291.1:g.15861C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1139C= MANE Select ENSP00000295897.4:p.Thr380=
ENST00000295897.8:c.1139C= ENSP00000295897.4:p.Thr380=
ENST00000401494.7:c.794C= ENSP00000384695.3:p.Thr265=
ENST00000415165.6:c.563C= ENSP00000401820.2:p.Thr188=
ENST00000476441.6:c.*418C= ENSP00000423727.1:n.*418C=
ENST00000484992.1:n.459C=
ENST00000503124.5:c.689C= ENSP00000421027.1:p.Thr230=
ENST00000504043.1:n.142C=
ENST00000505649.5:n.825C=
ENST00000509063.5:c.1139C= ENSP00000422784.1:p.Thr380=
ENST00000511370.1:c.672C=
ENST00000621085.4:c.500C= ENSP00000483421.1:p.Thr167=
ENST00000621628.4:c.500C= ENSP00000480485.1:p.Thr167=
NM_000477.5:c.1139C= NP_000468.1:p.Thr380=
NM_000477.6:c.1139C= NP_000468.1:p.Thr380=
NM_000477.7:c.1139C= MANE Select NP_000468.1:p.Thr380=