Canonical Allele Identifier: CA357235609
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406684A>T , CM000666.2:g.73406684A>T GRCh38
NC_000004.11:g.74272401A>T , CM000666.1:g.74272401A>T GRCh37
NC_000004.10:g.74491265A>T NCBI36
NG_009291.1:g.7430A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.193A>T MANE Select ENSP00000295897.4:p.Lys65Ter
ENST00000295897.8:c.193A>T ENSP00000295897.4:p.Lys65Ter
ENST00000401494.7:c.137+1511A>T ENSP00000384695.3:n.137+1511A>T
ENST00000415165.6:c.137+1511A>T ENSP00000401820.2:n.137+1511A>T
ENST00000441319.5:c.199A>T ENSP00000392541.1:p.Lys67Ter
ENST00000476441.6:c.79+2278A>T ENSP00000423727.1:n.79+2278A>T
ENST00000503124.5:c.-46A>T ENSP00000421027.1:n.-46A>T
ENST00000509063.5:c.193A>T ENSP00000422784.1:p.Lys65Ter
ENST00000510166.5:n.229A>T
ENST00000514786.1:n.162A>T
ENST00000515133.5:n.234A>T
ENST00000621085.4:c.193A>T ENSP00000483421.1:p.Lys65Ter
ENST00000621628.4:c.193A>T ENSP00000480485.1:p.Lys65Ter
NM_000477.5:c.193A>T NP_000468.1:p.Lys65Ter
NM_000477.6:c.193A>T NP_000468.1:p.Lys65Ter
NM_000477.7:c.193A>T MANE Select NP_000468.1:p.Lys65Ter