Canonical Allele Identifier: CA1468148428
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404313C= , CM000666.2:g.73404313C= GRCh38
NC_000004.11:g.74270030C= , CM000666.1:g.74270030C= GRCh37
NC_000004.10:g.74488894C= NCBI36
NG_009291.1:g.5059C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-15C= MANE Select ENSP00000295897.4:n.-15C=
ENST00000295897.8:c.-15C= ENSP00000295897.4:n.-15C=
ENST00000401494.7:c.-15C= ENSP00000384695.3:n.-15C=
ENST00000415165.6:c.-15C= ENSP00000401820.2:n.-15C=
ENST00000441319.5:n.48-56C= ENSP00000392541.1:n.48-56C=
ENST00000476441.6:c.-15C= ENSP00000423727.1:n.-15C=
ENST00000503124.5:c.-195C= ENSP00000421027.1:n.-195C=
ENST00000509063.5:c.-15C= ENSP00000422784.1:n.-15C=
ENST00000510166.5:n.27C=
ENST00000514786.1:n.25C=
ENST00000515133.5:n.27C=
ENST00000621085.4:c.-15C= ENSP00000483421.1:n.-15C=
ENST00000621628.4:c.-15C= ENSP00000480485.1:n.-15C=
NM_000477.5:c.-15C= NP_000468.1:n.-15C=
NM_000477.6:c.-15C= NP_000468.1:n.-15C=
NM_000477.7:c.-15C= MANE Select NP_000468.1:n.-15C=