Canonical Allele Identifier: CA1468150854
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406645G= , CM000666.2:g.73406645G= GRCh38
NC_000004.11:g.74272362G= , CM000666.1:g.74272362G= GRCh37
NC_000004.10:g.74491226G= NCBI36
NG_009291.1:g.7391G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.154G= MANE Select ENSP00000295897.4:p.Ala52=
ENST00000295897.8:c.154G= ENSP00000295897.4:p.Ala52=
ENST00000401494.7:c.137+1472G= ENSP00000384695.3:n.137+1472G=
ENST00000415165.6:c.137+1472G= ENSP00000401820.2:n.137+1472G=
ENST00000441319.5:c.160G= ENSP00000392541.1:p.Ala54=
ENST00000476441.6:c.79+2239G= ENSP00000423727.1:n.79+2239G=
ENST00000503124.5:c.-85G= ENSP00000421027.1:n.-85G=
ENST00000509063.5:c.154G= ENSP00000422784.1:p.Ala52=
ENST00000510166.5:n.190G=
ENST00000514786.1:n.123G=
ENST00000515133.5:n.195G=
ENST00000621085.4:c.154G= ENSP00000483421.1:p.Ala52=
ENST00000621628.4:c.154G= ENSP00000480485.1:p.Ala52=
NM_000477.5:c.154G= NP_000468.1:p.Ala52=
NM_000477.6:c.154G= NP_000468.1:p.Ala52=
NM_000477.7:c.154G= MANE Select NP_000468.1:p.Ala52=