Canonical Allele Identifier: CA798285069

Gene: ALB

Linked Data

• dbSNP Id: rs1297759575
• gnomAD v3: 4-73406845-CAAT-C
• gnomAD v4: 4-73406845-CAAT-C
• MyVariant Identifiers: chr4:g.74272563_74272565del (hg19) ; chr4:g.73406846_73406848del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406846_73406848del , CM000666.2:g.73406846_73406848del	GRCh38
NC_000004.11:g.74272563_74272565del , CM000666.1:g.74272563_74272565del	GRCh37
NC_000004.10:g.74491427_74491429del	NCBI36
NG_009291.1:g.7592_7594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+85_270+87del MANE Select	ENSP00000295897.4:n.270+85_270+87del
ENST00000295897.8:c.270+85_270+87del	ENSP00000295897.4:n.270+85_270+87del
ENST00000401494.7:c.137+1673_137+1675del	ENSP00000384695.3:n.137+1673_137+1675del
ENST00000415165.6:c.137+1673_137+1675del	ENSP00000401820.2:n.137+1673_137+1675del
ENST00000441319.5:c.276+85_276+87del	ENSP00000392541.1:n.276+85_276+87del
ENST00000476441.6:c.79+2440_79+2442del	ENSP00000423727.1:n.79+2440_79+2442del
ENST00000503124.5:c.32+85_32+87del	ENSP00000421027.1:n.32+85_32+87del
ENST00000509063.5:c.270+85_270+87del	ENSP00000422784.1:n.270+85_270+87del
ENST00000510166.5:n.306+85_306+87del
ENST00000514786.1:n.239+85_239+87del
ENST00000515133.5:n.311+85_311+87del
ENST00000621085.4:c.270+85_270+87del	ENSP00000483421.1:n.270+85_270+87del
ENST00000621628.4:c.270+85_270+87del	ENSP00000480485.1:n.270+85_270+87del
NM_000477.5:c.270+85_270+87del	NP_000468.1:n.270+85_270+87del
NM_000477.6:c.270+85_270+87del	NP_000468.1:n.270+85_270+87del
NM_000477.7:c.270+85_270+87del MANE Select	NP_000468.1:n.270+85_270+87del