Canonical Allele Identifier: CA357235539

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272386T>A (hg19) ; chr4:g.73406669T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406669T>A , CM000666.2:g.73406669T>A	GRCh38
NC_000004.11:g.74272386T>A , CM000666.1:g.74272386T>A	GRCh37
NC_000004.10:g.74491250T>A	NCBI36
NG_009291.1:g.7415T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.178T>A MANE Select	ENSP00000295897.4:p.Phe60Ile
ENST00000295897.8:c.178T>A	ENSP00000295897.4:p.Phe60Ile
ENST00000401494.7:c.137+1496T>A	ENSP00000384695.3:n.137+1496T>A
ENST00000415165.6:c.137+1496T>A	ENSP00000401820.2:n.137+1496T>A
ENST00000441319.5:c.184T>A	ENSP00000392541.1:p.Phe62Ile
ENST00000476441.6:c.79+2263T>A	ENSP00000423727.1:n.79+2263T>A
ENST00000503124.5:c.-61T>A	ENSP00000421027.1:n.-61T>A
ENST00000509063.5:c.178T>A	ENSP00000422784.1:p.Phe60Ile
ENST00000510166.5:n.214T>A
ENST00000514786.1:n.147T>A
ENST00000515133.5:n.219T>A
ENST00000621085.4:c.178T>A	ENSP00000483421.1:p.Phe60Ile
ENST00000621628.4:c.178T>A	ENSP00000480485.1:p.Phe60Ile
NM_000477.5:c.178T>A	NP_000468.1:p.Phe60Ile
NM_000477.6:c.178T>A	NP_000468.1:p.Phe60Ile
NM_000477.7:c.178T>A MANE Select	NP_000468.1:p.Phe60Ile