Canonical Allele Identifier: CA10621691

Gene: ALB

Linked Data

• ClinVar Variation Id: 349636
• ClinVar RCV Id: RCV000365417
• dbSNP Id: rs886059621
• MyVariant Identifiers: chr4:g.74283884A>T (hg19) ; chr4:g.73418167A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418167A>T , CM000666.2:g.73418167A>T	GRCh38
NC_000004.11:g.74283884A>T , CM000666.1:g.74283884A>T	GRCh37
NC_000004.10:g.74502748A>T	NCBI36
NG_009291.1:g.18913A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1508A>T MANE Select	ENSP00000295897.4:p.Glu503Val
ENST00000295897.8:c.1508A>T	ENSP00000295897.4:p.Glu503Val
ENST00000401494.7:c.1163A>T	ENSP00000384695.3:p.Glu388Val
ENST00000415165.6:c.932A>T	ENSP00000401820.2:p.Glu311Val
ENST00000476441.6:c.*787A>T	ENSP00000423727.1:n.*787A>T
ENST00000486939.1:n.162A>T
ENST00000503124.5:c.1058A>T	ENSP00000421027.1:p.Glu353Val
ENST00000505649.5:n.1055A>T
ENST00000509063.5:c.1508A>T	ENSP00000422784.1:p.Glu503Val
ENST00000511370.1:c.1041A>T
ENST00000621085.4:c.869A>T	ENSP00000483421.1:p.Glu290Val
ENST00000621628.4:c.869A>T	ENSP00000480485.1:p.Glu290Val
NM_000477.5:c.1508A>T	NP_000468.1:p.Glu503Val
NM_000477.6:c.1508A>T	NP_000468.1:p.Glu503Val
NM_000477.7:c.1508A>T MANE Select	NP_000468.1:p.Glu503Val