Canonical Allele Identifier: CA357236065
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406746T>G , CM000666.2:g.73406746T>G GRCh38
NC_000004.11:g.74272463T>G , CM000666.1:g.74272463T>G GRCh37
NC_000004.10:g.74491327T>G NCBI36
NG_009291.1:g.7492T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.255T>G MANE Select ENSP00000295897.4:p.Asn85Lys
ENST00000295897.8:c.255T>G ENSP00000295897.4:p.Asn85Lys
ENST00000401494.7:c.137+1573T>G ENSP00000384695.3:n.137+1573T>G
ENST00000415165.6:c.137+1573T>G ENSP00000401820.2:n.137+1573T>G
ENST00000441319.5:c.261T>G ENSP00000392541.1:p.Asn87Lys
ENST00000476441.6:c.79+2340T>G ENSP00000423727.1:n.79+2340T>G
ENST00000503124.5:c.17T>G ENSP00000421027.1:p.Ile6Ser
ENST00000509063.5:c.255T>G ENSP00000422784.1:p.Asn85Lys
ENST00000510166.5:n.291T>G
ENST00000514786.1:n.224T>G
ENST00000515133.5:n.296T>G
ENST00000621085.4:c.255T>G ENSP00000483421.1:p.Asn85Lys
ENST00000621628.4:c.255T>G ENSP00000480485.1:p.Asn85Lys
NM_000477.5:c.255T>G NP_000468.1:p.Asn85Lys
NM_000477.6:c.255T>G NP_000468.1:p.Asn85Lys
NM_000477.7:c.255T>G MANE Select NP_000468.1:p.Asn85Lys