Canonical Allele Identifier: CA1468151319

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73407090_73407094delinsGTATT , CM000666.2:g.73407090_73407094delinsGTATT	GRCh38
NC_000004.11:g.74272807_74272811delinsGTATT , CM000666.1:g.74272807_74272811delinsGTATT	GRCh37
NC_000004.10:g.74491671_74491675delinsGTATT	NCBI36
NG_009291.1:g.7836_7840delinsGTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+329_270+333delinsGTATT MANE Select	ENSP00000295897.4:n.270+329_270+333delinsGTATT
ENST00000295897.8:c.270+329_270+333delinsGTATT	ENSP00000295897.4:n.270+329_270+333delinsGTATT
ENST00000401494.7:c.137+1917_137+1921delinsGTATT	ENSP00000384695.3:n.137+1917_137+1921delinsGTATT
ENST00000415165.6:c.137+1917_137+1921delinsGTATT	ENSP00000401820.2:n.137+1917_137+1921delinsGTATT
ENST00000441319.5:c.276+329_276+333delinsGTATT	ENSP00000392541.1:n.276+329_276+333delinsGTATT
ENST00000476441.6:c.80-2265_80-2261delinsGTATT	ENSP00000423727.1:n.80-2265_80-2261delinsGTATT
ENST00000503124.5:c.32+329_32+333delinsGTATT	ENSP00000421027.1:n.32+329_32+333delinsGTATT
ENST00000509063.5:c.270+329_270+333delinsGTATT	ENSP00000422784.1:n.270+329_270+333delinsGTATT
ENST00000510166.5:n.306+329_306+333delinsGTATT
ENST00000514786.1:n.239+329_239+333delinsGTATT
ENST00000515133.5:n.311+329_311+333delinsGTATT
ENST00000621085.4:c.270+329_270+333delinsGTATT	ENSP00000483421.1:n.270+329_270+333delinsGTATT
ENST00000621628.4:c.270+329_270+333delinsGTATT	ENSP00000480485.1:n.270+329_270+333delinsGTATT
NM_000477.5:c.270+329_270+333delinsGTATT	NP_000468.1:n.270+329_270+333delinsGTATT
NM_000477.6:c.270+329_270+333delinsGTATT	NP_000468.1:n.270+329_270+333delinsGTATT
NM_000477.7:c.270+329_270+333delinsGTATT MANE Select	NP_000468.1:n.270+329_270+333delinsGTATT