Canonical Allele Identifier: CA439799448

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275123C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409406C>A , CM000666.2:g.73409406C>A	GRCh38
NC_000004.11:g.74275123C>A , CM000666.1:g.74275123C>A	GRCh37
NC_000004.10:g.74493987C>A	NCBI36
NG_009291.1:g.10152C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.534C>A MANE Select	ENSP00000295897.4:p.Leu178=
ENST00000295897.8:c.534C>A	ENSP00000295897.4:p.Leu178=
ENST00000401494.7:c.189C>A	ENSP00000384695.3:p.Leu63=
ENST00000415165.6:c.138-2590C>A	ENSP00000401820.2:n.138-2590C>A
ENST00000441319.5:c.540C>A	ENSP00000392541.1:p.Leu180=
ENST00000476441.6:c.131C>A	ENSP00000423727.1:p.Ser44Tyr
ENST00000503124.5:c.84C>A	ENSP00000421027.1:p.Leu28=
ENST00000505649.5:n.220C>A
ENST00000509063.5:c.534C>A	ENSP00000422784.1:p.Leu178=
ENST00000511370.1:c.67C>A
ENST00000514786.1:n.503C>A
ENST00000621085.4:c.490+44C>A	ENSP00000483421.1:n.490+44C>A
ENST00000621628.4:c.486+330C>A	ENSP00000480485.1:n.486+330C>A
NM_000477.5:c.534C>A	NP_000468.1:p.Leu178=
NM_000477.6:c.534C>A	NP_000468.1:p.Leu178=
NM_000477.7:c.534C>A MANE Select	NP_000468.1:p.Leu178=