Canonical Allele Identifier: CA648962704
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406854_73406856del , CM000666.2:g.73406854_73406856del GRCh38
NC_000004.11:g.74272571_74272573del , CM000666.1:g.74272571_74272573del GRCh37
NC_000004.10:g.74491435_74491437del NCBI36
NG_009291.1:g.7600_7602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.270+93_270+95del MANE Select ENSP00000295897.4:n.270+93_270+95del
ENST00000295897.8:c.270+93_270+95del ENSP00000295897.4:n.270+93_270+95del
ENST00000401494.7:c.137+1681_137+1683del ENSP00000384695.3:n.137+1681_137+1683del
ENST00000415165.6:c.137+1681_137+1683del ENSP00000401820.2:n.137+1681_137+1683del
ENST00000441319.5:c.276+93_276+95del ENSP00000392541.1:n.276+93_276+95del
ENST00000476441.6:c.79+2448_79+2450del ENSP00000423727.1:n.79+2448_79+2450del
ENST00000503124.5:c.32+93_32+95del ENSP00000421027.1:n.32+93_32+95del
ENST00000509063.5:c.270+93_270+95del ENSP00000422784.1:n.270+93_270+95del
ENST00000510166.5:n.306+93_306+95del
ENST00000514786.1:n.239+93_239+95del
ENST00000515133.5:n.311+93_311+95del
ENST00000621085.4:c.270+93_270+95del ENSP00000483421.1:n.270+93_270+95del
ENST00000621628.4:c.270+93_270+95del ENSP00000480485.1:n.270+93_270+95del
NM_000477.5:c.270+93_270+95del NP_000468.1:n.270+93_270+95del
NM_000477.6:c.270+93_270+95del NP_000468.1:n.270+93_270+95del
NM_000477.7:c.270+93_270+95del MANE Select NP_000468.1:n.270+93_270+95del