Canonical Allele Identifier: CA1468148461
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404330G= , CM000666.2:g.73404330G= GRCh38
NC_000004.11:g.74270047G= , CM000666.1:g.74270047G= GRCh37
NC_000004.10:g.74488911G= NCBI36
NG_009291.1:g.5076G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.3G= MANE Select ENSP00000295897.4:p.Met1=
ENST00000295897.8:c.3G= ENSP00000295897.4:p.Met1=
ENST00000401494.7:c.3G= ENSP00000384695.3:p.Met1=
ENST00000415165.6:c.3G= ENSP00000401820.2:p.Met1=
ENST00000441319.5:n.48-39G= ENSP00000392541.1:n.48-39G=
ENST00000476441.6:c.3G= ENSP00000423727.1:p.Met1=
ENST00000503124.5:c.-178G= ENSP00000421027.1:n.-178G=
ENST00000509063.5:c.3G= ENSP00000422784.1:p.Met1=
ENST00000510166.5:n.44G=
ENST00000514786.1:n.42G=
ENST00000515133.5:n.44G=
ENST00000621085.4:c.3G= ENSP00000483421.1:p.Met1=
ENST00000621628.4:c.3G= ENSP00000480485.1:p.Met1=
NM_000477.5:c.3G= NP_000468.1:p.Met1=
NM_000477.6:c.3G= NP_000468.1:p.Met1=
NM_000477.7:c.3G= MANE Select NP_000468.1:p.Met1=