Canonical Allele Identifier: CA1468151080

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406845_73406848delinsCAAT , CM000666.2:g.73406845_73406848delinsCAAT	GRCh38
NC_000004.11:g.74272562_74272565delinsCAAT , CM000666.1:g.74272562_74272565delinsCAAT	GRCh37
NC_000004.10:g.74491426_74491429delinsCAAT	NCBI36
NG_009291.1:g.7591_7594delinsCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+84_270+87delinsCAAT MANE Select	ENSP00000295897.4:n.270+84_270+87delinsCAAT
ENST00000295897.8:c.270+84_270+87delinsCAAT	ENSP00000295897.4:n.270+84_270+87delinsCAAT
ENST00000401494.7:c.137+1672_137+1675delinsCAAT	ENSP00000384695.3:n.137+1672_137+1675delinsCAAT
ENST00000415165.6:c.137+1672_137+1675delinsCAAT	ENSP00000401820.2:n.137+1672_137+1675delinsCAAT
ENST00000441319.5:c.276+84_276+87delinsCAAT	ENSP00000392541.1:n.276+84_276+87delinsCAAT
ENST00000476441.6:c.79+2439_79+2442delinsCAAT	ENSP00000423727.1:n.79+2439_79+2442delinsCAAT
ENST00000503124.5:c.32+84_32+87delinsCAAT	ENSP00000421027.1:n.32+84_32+87delinsCAAT
ENST00000509063.5:c.270+84_270+87delinsCAAT	ENSP00000422784.1:n.270+84_270+87delinsCAAT
ENST00000510166.5:n.306+84_306+87delinsCAAT
ENST00000514786.1:n.239+84_239+87delinsCAAT
ENST00000515133.5:n.311+84_311+87delinsCAAT
ENST00000621085.4:c.270+84_270+87delinsCAAT	ENSP00000483421.1:n.270+84_270+87delinsCAAT
ENST00000621628.4:c.270+84_270+87delinsCAAT	ENSP00000480485.1:n.270+84_270+87delinsCAAT
NM_000477.5:c.270+84_270+87delinsCAAT	NP_000468.1:n.270+84_270+87delinsCAAT
NM_000477.6:c.270+84_270+87delinsCAAT	NP_000468.1:n.270+84_270+87delinsCAAT
NM_000477.7:c.270+84_270+87delinsCAAT MANE Select	NP_000468.1:n.270+84_270+87delinsCAAT